StructureDefinition for substancesourcematerial Example of evidencereport

@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .


Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource
       (including cannot change the meaning of modifierExtension itself).
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      Modifier extensions allow for extensions that *cannot* be safely ignored to be clearly
       distinguished from the vast majority of extensions which can be safely ignored.  This
       promotes interoperability by eliminating the need for implementers to prohibit the presence
       of extensions. For further information, see the [definition of modifier extensions](extensibility.ht
      ml#modifierExtension).
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      Modifier extensions are expected to modify the meaning or interpretation of the resource
       that contains them
      
      
        
        
      
    
    
      
      General high level classification of the source material specific to the origin of the
       material
      General high level classification of the source material specific to the origin of the
       material.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The type of the source material shall be specified based on a controlled vocabulary. For
       vaccines, this subclause refers to the class of infectious agent
      The type of the source material shall be specified based on a controlled vocabulary. For
       vaccines, this subclause refers to the class of infectious agent.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The parent of the herbal drug Ginkgo biloba, Leaf is the substance ID of the substance
       (fresh) of Ginkgo biloba L. or Ginkgo biloba L. (Whole plant)
      The parent of the herbal drug Ginkgo biloba, Leaf is the substance ID of the substance
       (fresh) of Ginkgo biloba L. or Ginkgo biloba L. (Whole plant).
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The country where the plant material is harvested or the countries where the plasma is
       sourced from as laid down in accordance with the Plasma Master File. For “Plasma-derived
       substances� the attribute country of origin provides information about the countries used
       for the manufacturing of the Cryopoor plama or Crioprecipitate
      The country where the plant material is harvested or the countries where the plasma is
       sourced from as laid down in accordance with the Plasma Master File. For “Plasma-derived
       substances� the attribute country of origin provides information about the countries used
       for the manufacturing of the Cryopoor plama or Crioprecipitate.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The place/region where the plant is harvested or the places/regions where the animal source
       material has its habitat
      The place/region where the plant is harvested or the places/regions where the animal source
       material has its habitat.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      Stage of life for animals, plants, insects and microorganisms. This information shall
       be provided only when the substance is significantly different in these stages (e.g. foetal
       bovine serum)
      Stage of life for animals, plants, insects and microorganisms. This information shall
       be provided only when the substance is significantly different in these stages (e.g. foetal
       bovine serum).
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      Many complex materials are fractions of parts of plants, animals, or minerals. Fraction
       elements are often necessary to define both Substances and Specified Group 1 Substances.
       For substances derived from Plants, fraction information will be captured at the Substance
       information level ( . Oils, Juices and Exudates). Additional information for Extracts,
       such as extraction solvent composition, will be captured at the Specified Substance Group
       1 information level. For plasma-derived products fraction information will be captured
       at the Substance and the Specified Substance Group 1 levels
      Many complex materials are fractions of parts of plants, animals, or minerals. Fraction
       elements are often necessary to define both Substances and Specified Group 1 Substances.
       For substances derived from Plants, fraction information will be captured at the Substance
       information level ( . Oils, Juices and Exudates). Additional information for Extracts,
       such as extraction solvent composition, will be captured at the Specified Substance Group
       1 information level. For plasma-derived products fraction information will be captured
       at the Substance and the Specified Substance Group 1 levels.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      Unique id for the element within a resource (for internal references). This may be any
       string value that does not contain spaces.
      
      
      
        
        
        
      
    <!--  Note: special primitive values have a FHIRPath system type. e.g. this is compiler magic
       (j)  -->
      
        
          
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element. To make the use of extensions safe and manageable, there is a strict set
       of governance  applied to the definition and use of extensions. Though any implementer
       can define an extension, there is a set of requirements that SHALL be met as part of the
       definition of the extension.
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element and that modifies the understanding of the element in which it is contained
       and/or the understanding of the containing element's descendants. Usually modifier elements
       provide negation or qualification. To make the use of extensions safe and manageable,
       there is a strict set of governance applied to the definition and use of extensions. Though
       any implementer can define an extension, there is a set of requirements that SHALL be
       met as part of the definition of the extension. Applications processing a resource are
       required to check for modifier extensions.

# - resource -------------------------------------------------------------------


Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource
       (including cannot change the meaning of modifierExtension itself).
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      Modifier extensions allow for extensions that *cannot* be safely ignored to be clearly
       distinguished from the vast majority of extensions which can be safely ignored.  This
       promotes interoperability by eliminating the need for implementers to prohibit the presence
       of extensions. For further information, see the [definition of modifier extensions](extensibility.ht
      ml#modifierExtension).
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      Modifier extensions are expected to modify the meaning or interpretation of the element
       that contains them
      
      
        
        
      
    
    
      
      This element is capturing information about the fraction of a plant part, or human plasma
       for fractionation
      This element is capturing information about the fraction of a plant part, or human plasma
       for fractionation.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The specific type of the material constituting the component. For Herbal preparations
       the particulars of the extracts (liquid/dry) is described in Specified Substance Group
       1
      The specific type of the material constituting the component. For Herbal preparations
       the particulars of the extracts (liquid/dry) is described in Specified Substance Group
       1.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      This subclause describes the organism which the substance is derived from. For vaccines,
       the parent organism shall be specified based on these subclause elements. As an example,
       full taxonomy will be described for the Substance Name: ., Leaf
      This subclause describes the organism which the substance is derived from. For vaccines,
       the parent organism shall be specified based on these subclause elements. As an example,
       full taxonomy will be described for the Substance Name: ., Leaf.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      Unique id for the element within a resource (for internal references). This may be any
       string value that does not contain spaces.
      
      
      
        
        
        
      
    <!--  Note: special primitive values have a FHIRPath system type. e.g. this is compiler magic
       (j)  -->
      
        
          
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element. To make the use of extensions safe and manageable, there is a strict set
       of governance  applied to the definition and use of extensions. Though any implementer
       can define an extension, there is a set of requirements that SHALL be met as part of the
       definition of the extension.
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element and that modifies the understanding of the element in which it is contained
       and/or the understanding of the containing element's descendants. Usually modifier elements
       provide negation or qualification. To make the use of extensions safe and manageable,
       there is a strict set of governance applied to the definition and use of extensions. Though
       any implementer can define an extension, there is a set of requirements that SHALL be
       met as part of the definition of the extension. Applications processing a resource are
       required to check for modifier extensions.

[a fhir:EvidenceReport;
  fhir:nodeRole fhir:treeRoot;
  fhir:Resource.id [ fhir:value "example"]; # 
  fhir:DomainResource.text [
     fhir:Narrative.status [ fhir:value "generated" ];
     fhir:Narrative.div "<div xmlns=\"http://www.w3.org/1999/xhtml\">[Put rendering here]</div>"
  ]; # 
  fhir:EvidenceReport.status [ fhir:value "draft"]; # 
  fhir:EvidenceReport.subject [
     fhir:EvidenceReport.subject.note [
       fhir:index 0;
       fhir:Annotation.text [ fhir:value "This is just an example." ]
     ]
  ]] . # 


Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource
       (including cannot change the meaning of modifierExtension itself).
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      Modifier extensions allow for extensions that *cannot* be safely ignored to be clearly
       distinguished from the vast majority of extensions which can be safely ignored.  This
       promotes interoperability by eliminating the need for implementers to prohibit the presence
       of extensions. For further information, see the [definition of modifier extensions](extensibility.ht
      ml#modifierExtension).
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      Modifier extensions are expected to modify the meaning or interpretation of the element
       that contains them
      
      
        
        
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The genus of an organism shall be specified; refers to the Latin epithet of the genus
       element of the plant/animal scientific name; it is present in names for genera, species
       and infraspecies
      The genus of an organism shall be specified; refers to the Latin epithet of the genus
       element of the plant/animal scientific name; it is present in names for genera, species
       and infraspecies.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The species of an organism shall be specified; refers to the Latin epithet of the species
       of the plant/animal; it is present in names for species and infraspecies
      The species of an organism shall be specified; refers to the Latin epithet of the species
       of the plant/animal; it is present in names for species and infraspecies.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The intraspecific description of an organism shall be specified based on a controlled
       vocabulary. For Influenza Vaccine, the intraspecific description shall contain the syntax
       of the antigen in line with the WHO convention
      The intraspecific description of an organism shall be specified based on a controlled
       vocabulary. For Influenza Vaccine, the intraspecific description shall contain the syntax
       of the antigen in line with the WHO convention.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      Unique id for the element within a resource (for internal references). This may be any
       string value that does not contain spaces.
      
      
      
        
        
        
      
    <!--  Note: special primitive values have a FHIRPath system type. e.g. this is compiler magic
       (j)  -->
      
        
          
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element. To make the use of extensions safe and manageable, there is a strict set
       of governance  applied to the definition and use of extensions. Though any implementer
       can define an extension, there is a set of requirements that SHALL be met as part of the
       definition of the extension.
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element and that modifies the understanding of the element in which it is contained
       and/or the understanding of the containing element's descendants. Usually modifier elements
       provide negation or qualification. To make the use of extensions safe and manageable,
       there is a strict set of governance applied to the definition and use of extensions. Though
       any implementer can define an extension, there is a set of requirements that SHALL be
       met as part of the definition of the extension. Applications processing a resource are
       required to check for modifier extensions.

# - ontology header ------------------------------------------------------------


Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource
       (including cannot change the meaning of modifierExtension itself).
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      Modifier extensions allow for extensions that *cannot* be safely ignored to be clearly
       distinguished from the vast majority of extensions which can be safely ignored.  This
       promotes interoperability by eliminating the need for implementers to prohibit the presence
       of extensions. For further information, see the [definition of modifier extensions](extensibility.ht
      ml#modifierExtension).
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      Modifier extensions are expected to modify the meaning or interpretation of the element
       that contains them
      
      
        
        
      
    
    
      
      The type of author of an organism species shall be specified. The parenthetical author
       of an organism species refers to the first author who published the plant/animal name
       (of any rank). The primary author of an organism species refers to the first author(s),
       who validly published the plant/animal name
      The type of author of an organism species shall be specified. The parenthetical author
       of an organism species refers to the first author who published the plant/animal name
       (of any rank). The primary author of an organism species refers to the first author(s),
       who validly published the plant/animal name.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The author of an organism species shall be specified. The author year of an organism shall
       also be specified when applicable; refers to the year in which the first author(s) published
       the infraspecific plant/animal name (of any rank)
      The author of an organism species shall be specified. The author year of an organism shall
       also be specified when applicable; refers to the year in which the first author(s) published
       the infraspecific plant/animal name (of any rank).
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      Unique id for the element within a resource (for internal references). This may be any
       string value that does not contain spaces.
      
      
      
        
        
        
      
    <!--  Note: special primitive values have a FHIRPath system type. e.g. this is compiler magic
       (j)  -->
      
        
          
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element. To make the use of extensions safe and manageable, there is a strict set
       of governance  applied to the definition and use of extensions. Though any implementer
       can define an extension, there is a set of requirements that SHALL be met as part of the
       definition of the extension.
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element and that modifies the understanding of the element in which it is contained
       and/or the understanding of the containing element's descendants. Usually modifier elements
       provide negation or qualification. To make the use of extensions safe and manageable,
       there is a strict set of governance applied to the definition and use of extensions. Though
       any implementer can define an extension, there is a set of requirements that SHALL be
       met as part of the definition of the extension. Applications processing a resource are
       required to check for modifier extensions.

[a owl:Ontology;
  owl:imports fhir:fhir.ttl] .


Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource
       (including cannot change the meaning of modifierExtension itself).
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      Modifier extensions allow for extensions that *cannot* be safely ignored to be clearly
       distinguished from the vast majority of extensions which can be safely ignored.  This
       promotes interoperability by eliminating the need for implementers to prohibit the presence
       of extensions. For further information, see the [definition of modifier extensions](extensibility.ht
      ml#modifierExtension).
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      Modifier extensions are expected to modify the meaning or interpretation of the element
       that contains them
      
      
        
        
      
    
    
      
      The identifier of the maternal species constituting the hybrid organism shall be specified
       based on a controlled vocabulary. For plants, the parents aren’t always known, and it
       is unlikely that it will be known which is maternal and which is paternal
      The identifier of the maternal species constituting the hybrid organism shall be specified
       based on a controlled vocabulary. For plants, the parents aren’t always known, and it
       is unlikely that it will be known which is maternal and which is paternal.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The name of the maternal species constituting the hybrid organism shall be specified.
       For plants, the parents aren’t always known, and it is unlikely that it will be known
       which is maternal and which is paternal
      The name of the maternal species constituting the hybrid organism shall be specified.
       For plants, the parents aren’t always known, and it is unlikely that it will be known
       which is maternal and which is paternal.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The identifier of the paternal species constituting the hybrid organism shall be specified
       based on a controlled vocabulary
      The identifier of the paternal species constituting the hybrid organism shall be specified
       based on a controlled vocabulary.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      Unique id for the element within a resource (for internal references). This may be any
       string value that does not contain spaces.
      
      
      
        
        
        
      
    <!--  Note: special primitive values have a FHIRPath system type. e.g. this is compiler magic
       (j)  -->
      
        
          
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element. To make the use of extensions safe and manageable, there is a strict set
       of governance  applied to the definition and use of extensions. Though any implementer
       can define an extension, there is a set of requirements that SHALL be met as part of the
       definition of the extension.
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element and that modifies the understanding of the element in which it is contained
       and/or the understanding of the containing element's descendants. Usually modifier elements
       provide negation or qualification. To make the use of extensions safe and manageable,
       there is a strict set of governance applied to the definition and use of extensions. Though
       any implementer can define an extension, there is a set of requirements that SHALL be
       met as part of the definition of the extension. Applications processing a resource are
       required to check for modifier extensions.

# -------------------------------------------------------------------------------------


Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource
       (including cannot change the meaning of modifierExtension itself).
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      Modifier extensions allow for extensions that *cannot* be safely ignored to be clearly
       distinguished from the vast majority of extensions which can be safely ignored.  This
       promotes interoperability by eliminating the need for implementers to prohibit the presence
       of extensions. For further information, see the [definition of modifier extensions](extensibility.ht
      ml#modifierExtension).
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      Modifier extensions are expected to modify the meaning or interpretation of the element
       that contains them
      
      
        
        
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      
      
      Unique id for the element within a resource (for internal references). This may be any
       string value that does not contain spaces.
      
      
      
        
        
        
      
    <!--  Note: special primitive values have a FHIRPath system type. e.g. this is compiler magic
       (j)  -->
      
        
          
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element. To make the use of extensions safe and manageable, there is a strict set
       of governance  applied to the definition and use of extensions. Though any implementer
       can define an extension, there is a set of requirements that SHALL be met as part of the
       definition of the extension.
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      
      
        
        
      
    
    
      
      
      May be used to represent additional information that is not part of the basic definition
       of the element and that modifies the understanding of the element in which it is contained
       and/or the understanding of the containing element's descendants. Usually modifier elements
       provide negation or qualification. To make the use of extensions safe and manageable,
       there is a strict set of governance applied to the definition and use of extensions. Though
       any implementer can define an extension, there is a set of requirements that SHALL be
       met as part of the definition of the extension. Applications processing a resource are
       required to check for modifier extensions.


Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource
       (including cannot change the meaning of modifierExtension itself).
      There can be no stigma associated with the use of extensions by any application, project,
       or standard - regardless of the institution or jurisdiction that uses or defines the extensions.
        The use of extensions is what allows the FHIR specification to retain a core level of
       simplicity for everyone.
      Modifier extensions allow for extensions that *cannot* be safely ignored to be clearly
       distinguished from the vast majority of extensions which can be safely ignored.  This
       promotes interoperability by eliminating the need for implementers to prohibit the presence
       of extensions. For further information, see the [definition of modifier extensions](extensibility.ht
      ml#modifierExtension).
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
        
        
        
        
        
        
      
      
      Modifier extensions are expected to modify the meaning or interpretation of the element
       that contains them
      
      
        
        
      
    
    
      
      
      
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
    
      
      The detailed anatomic location when the part can be extracted from different anatomical
       locations of the organism. Multiple alternative locations may apply
      The detailed anatomic location when the part can be extracted from different anatomical
       locations of the organism. Multiple alternative locations may apply.
      
      
      
        
        
        
      
      
        
      
      
        
        
        
        
        
        
      
      
      
    
  
  
    
      
      Source material shall capture information on the taxonomic and anatomical origins as well
       as the fraction of a material that can result in or can be modified to form a substance.
       This set of data elements shall be used to define polymer substances isolated from biological
       matrices. Taxonomic and anatomical origins shall be described using a controlled vocabulary
       as required. This information is captured for naturally derived polymers ( . starch) and
       structurally diverse substances. For Organisms belonging to the Kingdom Plantae the Substance
       level defines the fresh material of a single species or infraspecies, the Herbal Drug
       and the Herbal preparation. For Herbal preparations, the fraction information will be
       captured at the Substance information level and additional information for herbal extracts
       will be captured at the Specified Substance Group 1 information level. See for further
       explanation the Substance Class: Structurally Diverse and the herbal annex
      Source material shall capture information on the taxonomic and anatomical origins as well
       as the fraction of a material that can result in or can be modified to form a substance.
       This set of data elements shall be used to define polymer substances isolated from biological
       matrices. Taxonomic and anatomical origins shall be described using a controlled vocabulary
       as required. This information is captured for naturally derived polymers ( . starch) and
       structurally diverse substances. For Organisms belonging to the Kingdom Plantae the Substance
       level defines the fresh material of a single species or infraspecies, the Herbal Drug
       and the Herbal preparation. For Herbal preparations, the fraction information will be
       captured at the Substance information level and additional information for herbal extracts
       will be captured at the Specified Substance Group 1 information level. See for further
       explanation the Substance Class: Structurally Diverse and the herbal annex.
      
      
    
    
      
      General high level classification of the source material specific to the origin of the
       material
      General high level classification of the source material specific to the origin of the
       material.
      
      
      
        
      
      
    
    
      
      The type of the source material shall be specified based on a controlled vocabulary. For
       vaccines, this subclause refers to the class of infectious agent
      The type of the source material shall be specified based on a controlled vocabulary. For
       vaccines, this subclause refers to the class of infectious agent.
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      The parent of the herbal drug Ginkgo biloba, Leaf is the substance ID of the substance
       (fresh) of Ginkgo biloba L. or Ginkgo biloba L. (Whole plant)
      The parent of the herbal drug Ginkgo biloba, Leaf is the substance ID of the substance
       (fresh) of Ginkgo biloba L. or Ginkgo biloba L. (Whole plant).
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      The country where the plant material is harvested or the countries where the plasma is
       sourced from as laid down in accordance with the Plasma Master File. For “Plasma-derived
       substances� the attribute country of origin provides information about the countries used
       for the manufacturing of the Cryopoor plama or Crioprecipitate
      The country where the plant material is harvested or the countries where the plasma is
       sourced from as laid down in accordance with the Plasma Master File. For “Plasma-derived
       substances� the attribute country of origin provides information about the countries used
       for the manufacturing of the Cryopoor plama or Crioprecipitate.
      
      
      
        
      
      
    
    
      
      The place/region where the plant is harvested or the places/regions where the animal source
       material has its habitat
      The place/region where the plant is harvested or the places/regions where the animal source
       material has its habitat.
      
      
      
        
      
      
    
    
      
      Stage of life for animals, plants, insects and microorganisms. This information shall
       be provided only when the substance is significantly different in these stages (e.g. foetal
       bovine serum)
      Stage of life for animals, plants, insects and microorganisms. This information shall
       be provided only when the substance is significantly different in these stages (e.g. foetal
       bovine serum).
      
      
      
        
      
      
    
    
      
      Many complex materials are fractions of parts of plants, animals, or minerals. Fraction
       elements are often necessary to define both Substances and Specified Group 1 Substances.
       For substances derived from Plants, fraction information will be captured at the Substance
       information level ( . Oils, Juices and Exudates). Additional information for Extracts,
       such as extraction solvent composition, will be captured at the Specified Substance Group
       1 information level. For plasma-derived products fraction information will be captured
       at the Substance and the Specified Substance Group 1 levels
      Many complex materials are fractions of parts of plants, animals, or minerals. Fraction
       elements are often necessary to define both Substances and Specified Group 1 Substances.
       For substances derived from Plants, fraction information will be captured at the Substance
       information level ( . Oils, Juices and Exudates). Additional information for Extracts,
       such as extraction solvent composition, will be captured at the Specified Substance Group
       1 information level. For plasma-derived products fraction information will be captured
       at the Substance and the Specified Substance Group 1 levels.
      
      
      
        
      
      
    
    
      
      This element is capturing information about the fraction of a plant part, or human plasma
       for fractionation
      This element is capturing information about the fraction of a plant part, or human plasma
       for fractionation.
      
      
      
        
      
      
    
    
      
      The specific type of the material constituting the component. For Herbal preparations
       the particulars of the extracts (liquid/dry) is described in Specified Substance Group
       1
      The specific type of the material constituting the component. For Herbal preparations
       the particulars of the extracts (liquid/dry) is described in Specified Substance Group
       1.
      
      
      
        
      
      
    
    
      
      This subclause describes the organism which the substance is derived from. For vaccines,
       the parent organism shall be specified based on these subclause elements. As an example,
       full taxonomy will be described for the Substance Name: ., Leaf
      This subclause describes the organism which the substance is derived from. For vaccines,
       the parent organism shall be specified based on these subclause elements. As an example,
       full taxonomy will be described for the Substance Name: ., Leaf.
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      The genus of an organism shall be specified; refers to the Latin epithet of the genus
       element of the plant/animal scientific name; it is present in names for genera, species
       and infraspecies
      The genus of an organism shall be specified; refers to the Latin epithet of the genus
       element of the plant/animal scientific name; it is present in names for genera, species
       and infraspecies.
      
      
      
        
      
      
    
    
      
      The species of an organism shall be specified; refers to the Latin epithet of the species
       of the plant/animal; it is present in names for species and infraspecies
      The species of an organism shall be specified; refers to the Latin epithet of the species
       of the plant/animal; it is present in names for species and infraspecies.
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      The intraspecific description of an organism shall be specified based on a controlled
       vocabulary. For Influenza Vaccine, the intraspecific description shall contain the syntax
       of the antigen in line with the WHO convention
      The intraspecific description of an organism shall be specified based on a controlled
       vocabulary. For Influenza Vaccine, the intraspecific description shall contain the syntax
       of the antigen in line with the WHO convention.
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      The type of author of an organism species shall be specified. The parenthetical author
       of an organism species refers to the first author who published the plant/animal name
       (of any rank). The primary author of an organism species refers to the first author(s),
       who validly published the plant/animal name
      The type of author of an organism species shall be specified. The parenthetical author
       of an organism species refers to the first author who published the plant/animal name
       (of any rank). The primary author of an organism species refers to the first author(s),
       who validly published the plant/animal name.
      
      
      
        
      
      
    
    
      
      The author of an organism species shall be specified. The author year of an organism shall
       also be specified when applicable; refers to the year in which the first author(s) published
       the infraspecific plant/animal name (of any rank)
      The author of an organism species shall be specified. The author year of an organism shall
       also be specified when applicable; refers to the year in which the first author(s) published
       the infraspecific plant/animal name (of any rank).
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      The identifier of the maternal species constituting the hybrid organism shall be specified
       based on a controlled vocabulary. For plants, the parents aren’t always known, and it
       is unlikely that it will be known which is maternal and which is paternal
      The identifier of the maternal species constituting the hybrid organism shall be specified
       based on a controlled vocabulary. For plants, the parents aren’t always known, and it
       is unlikely that it will be known which is maternal and which is paternal.
      
      
      
        
      
      
    
    
      
      The name of the maternal species constituting the hybrid organism shall be specified.
       For plants, the parents aren’t always known, and it is unlikely that it will be known
       which is maternal and which is paternal
      The name of the maternal species constituting the hybrid organism shall be specified.
       For plants, the parents aren’t always known, and it is unlikely that it will be known
       which is maternal and which is paternal.
      
      
      
        
      
      
    
    
      
      The identifier of the paternal species constituting the hybrid organism shall be specified
       based on a controlled vocabulary
      The identifier of the paternal species constituting the hybrid organism shall be specified
       based on a controlled vocabulary.
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      
      
      
      
      
        
      
      
    
    
      
      The detailed anatomic location when the part can be extracted from different anatomical
       locations of the organism. Multiple alternative locations may apply
      The detailed anatomic location when the part can be extracted from different anatomical
       locations of the organism. Multiple alternative locations may apply.
      
      
      
        
      
      
    
  
</
StructureDefinition
>