Breast cancer risk assessment

@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#> .

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

[a fhir:RiskAssessment ;
  fhir:nodeRole fhir:treeRoot ;
  fhir:id [ fhir:v "breastcancer-risk"] ; # 
  fhir:text [
     fhir:status [ fhir:v "additional" ] ;
     fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\">\n      <table>\n        <tr>\n          <td colspan=\"2\">\n            <h1>Information about your risk score:</h1>\n          </td>\n        </tr>\n        <tr>\n          <td>\n            <strong>Birthdate:</strong>\n          </td>\n          <td>1981-01-01</td>\n        </tr>\n        <tr>\n          <td>\n            <strong>Gender:</strong>\n          </td>\n          <td>female</td>\n        </tr>\n        <tr>\n          <td>\n            <strong>Ethnicity:</strong>\n          </td>\n          <td>Unknown / Not Reported</td>\n        </tr>\n      </table>\n    </div>"
  ] ; # 
  fhir:identifier ( [
     fhir:use [ fhir:v "official" ] ;
     fhir:system [ fhir:v "http://example.org"^^xsd:anyURI ] ;
     fhir:value [ fhir:v "risk-assessment-breastcancer1" ]
  ] ) ; # 
  fhir:status [ fhir:v "final"] ; # 
  fhir:code [
     fhir:coding ( [
       fhir:system [ fhir:v "http://browser.ihtsdotools.org/"^^xsd:anyURI ] ;
       fhir:code [ fhir:v "709510001" ] ;
       fhir:display [ fhir:v "Assessment of risk for disease (procedure)" ]
     ] )
  ] ; # 
  fhir:subject [
     fhir:reference [ fhir:v "Patient/example" ]
  ] ; # 
  fhir:performer [
     fhir:reference [ fhir:v "Practitioner/example" ]
  ] ; # 
  fhir:basis ( [
     fhir:reference [ fhir:v "Observation/example-genetics-brcapat" ]
  ] ) ; # 
  fhir:prediction ( [
     fhir:outcome [
       fhir:text [ fhir:v "Unknown risk of developing breast cancer" ]
     ]
  ] ) ; # 
  fhir:note ( [
     fhir:text [ fhir:v "This risk assessment is based on BRCA1 and BRCA2 genetic mutation test" ]
  ] )] . # 

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