Vital Records Birth and Fetal Death Reporting
0.1.0 - STU 1 Ballot

This page is part of the Vital Records Birth and Fetal Death Reporting (v0.1.0: STU 1 on FHIR R4 Ballot 1) based on FHIR R4. The current version which supercedes this version is 1.0.0. For a full list of available versions, see the Directory of published versions

: Condition - Congenital Anomaly of Newborn example [Baby G Quinn] - TTL Representation

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

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

 a fhir:Condition;
  fhir:nodeRole fhir:treeRoot;
  fhir:Resource.id [ fhir:value "condition-congenital-anomaly-of-newborn-babyg-quinn-2"];
  fhir:Resource.meta [
     fhir:Meta.versionId [ fhir:value "2" ];
     fhir:Meta.lastUpdated [ fhir:value "2020-08-20T23:20:37.897+00:00"^^xsd:dateTime ];
     fhir:Meta.source [ fhir:value "#8nHKxfsyONG1qyLw" ];
     fhir:Meta.profile [
       fhir:value "http://hl7.org/fhir/us/bfdr/StructureDefinition/Condition-congenital-anomaly-of-newborn";
       fhir:index 0;
       fhir:link <http://hl7.org/fhir/us/bfdr/StructureDefinition/Condition-congenital-anomaly-of-newborn>     ]
  ];
  fhir:DomainResource.text [
     fhir:Narrative.status [ fhir:value "generated" ];
     fhir:Narrative.div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative</b></p><p><b>category</b>: <span title=\"Codes: {http://loinc.org 73780-9}\">Congenital anomalies of the newborn [US Standard Certificate of Live Birth]</span></p><p><b>code</b>: <span title=\"Codes: {http://snomed.info/sct 70156005}\">Anomaly of chromosome pair 21 (disorder)</span></p><p><b>subject</b>: <a href=\"Patient-patient-child-babyg-quinn.html\">Patient - Child (Baby G Quinn). Generated Summary: Medical Record Number: 9932702 (USUAL); Baby G Quinn ; gender: female; birthDate: 2019-02-12; 1</a></p><h3>Evidences</h3><table class=\"grid\"><tr><td>-</td><td><b>Code</b></td></tr><tr><td>*</td><td><span title=\"Codes: {http://snomed.info/sct 312948004}\">Karyotype determination pending</span></td></tr></table></div>"
  ];
  fhir:Condition.category [
     fhir:index 0;
     fhir:CodeableConcept.coding [
       fhir:index 0;
       a loinc:73780-9;
       fhir:Coding.system [ fhir:value "http://loinc.org" ];
       fhir:Coding.code [ fhir:value "73780-9" ];
       fhir:Coding.display [ fhir:value "Congenital anomalies of the newborn [US Standard Certificate of Live Birth]" ]     ]
  ];
  fhir:Condition.code [
     fhir:CodeableConcept.coding [
       fhir:index 0;
       a sct:70156005;
       fhir:Coding.system [ fhir:value "http://snomed.info/sct" ];
       fhir:Coding.code [ fhir:value "70156005" ];
       fhir:Coding.display [ fhir:value "Anomaly of chromosome pair 21 (disorder)" ]     ];
     fhir:CodeableConcept.text [ fhir:value "Anomaly of chromosome pair 21 (disorder)" ]
  ];
  fhir:Condition.subject [
     fhir:Reference.reference [ fhir:value "Patient/patient-child-babyg-quinn" ];
     fhir:Reference.display [ fhir:value "Patient - Child (Baby G Quinn)" ]
  ];
  fhir:Condition.evidence [
     fhir:index 0;
     fhir:Condition.evidence.code [
       fhir:index 0;
       fhir:CodeableConcept.coding [
         fhir:index 0;
         a sct:312948004;
         fhir:Coding.system [ fhir:value "http://snomed.info/sct" ];
         fhir:Coding.code [ fhir:value "312948004" ];
         fhir:Coding.display [ fhir:value "Karyotype determination" ]       ];
       fhir:CodeableConcept.text [ fhir:value "Karyotype determination pending" ]     ]
  ].

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

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