FHIR IG analytics

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Source1

{
  "resourceType": "Task",
  "id": "Task-FollowupRecommendationReport-Example",
  "meta": {
    "profile": [
      "http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/followup-recommendation"
    ]
  },
  "status": "requested",
  "intent": "proposal",
  "code": {
    "coding": [
      {
        "system": "http://loinc.org",
        "code": "LA14021-2",
        "display": "Confirmatory testing recommended"
      }
    ]
  },
  "description": "Testing of Pheobe's parents is recommended (via referral to the clinical genetics service) in order to confirm that both are heterozygous carriers of the missense variant.",
  "for": {
    "reference": "Patient/Patient-PheobeSmitham-Example"
  },
  "reasonReference": {
    "reference": "Observation/Observation-GenomicTherapeuticImplication-Example"
  },
  "input": [
    {
      "type": {
        "coding": [
          {
            "system": "http://terminology.hl7.org/CodeSystem/v3-RoleCode",
            "code": "NFTH",
            "display": "natural father"
          }
        ]
      },
      "valueReference": {
        "reference": "Patient/Patient-PheobeSmithamFather-Example"
      }
    },
    {
      "type": {
        "coding": [
          {
            "system": "http://terminology.hl7.org/CodeSystem/v3-RoleCode",
            "code": "NMTH",
            "display": "natural mother"
          }
        ]
      },
      "valueReference": {
        "reference": "Patient/Patient-PheobeSmithamMother-Example"
      }
    }
  ]
}