This page is part of the FHIR Specification (v3.2.0: R4 Ballot 1). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B R4
Clinical Genomics Work Group | Maturity Level: N/A | Ballot Status: Informative | Compartments: Not linked to any defined compartments |
Sequence example for patient with breast cancer gene variant
@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 ------------------------------------------------------------------- <http://hl7.org/fhir/Sequence/breastcancer> a fhir:Sequence; fhir:nodeRole fhir:treeRoot; fhir:Resource.id [ fhir:value "breastcancer"]; fhir:DomainResource.text [ fhir:Narrative.status [ fhir:value "generated" ]; fhir:Narrative.div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: breastcancer</p><p><b>type</b>: rna</p><p><b>coordinateSystem</b>: 0</p><p><b>patient</b>: <a>Patient/brcapat</a></p><h3>ReferenceSeqs</h3><table><tr><td>-</td><td><b>ReferenceSeqId</b></td><td><b>WindowStart</b></td><td><b>WindowEnd</b></td></tr><tr><td>*</td><td>Homo sapiens BRCA2, DNA repair associated (BRCA2), mRNA <span>(Details : {http://www.ncbi.nlm.nih.gov/nuccore/ code 'NM_000059.3' = 'NM_000059.3', given as 'Homo sapiens BRCA2, DNA repair associated (BRCA2), mRNA'})</span></td><td>101488058</td><td>101499444</td></tr></table><h3>Variants</h3><table><tr><td>-</td><td><b>Start</b></td><td><b>End</b></td><td><b>ObservedAllele</b></td><td><b>ReferenceAllele</b></td></tr><tr><td>*</td><td>32316186</td><td>32316187</td><td>A</td><td>C</td></tr></table></div>" ]; fhir:Sequence.type [ fhir:value "rna"]; fhir:Sequence.coordinateSystem [ fhir:value "0"^^xsd:integer]; fhir:Sequence.patient [ fhir:link <http://hl7.org/fhir/Patient/brcapat>; fhir:Reference.reference [ fhir:value "Patient/brcapat" ] ]; fhir:Sequence.referenceSeq [ fhir:Sequence.referenceSeq.referenceSeqId [ fhir:CodeableConcept.coding [ fhir:index 0; fhir:Coding.system [ fhir:value "http://www.ncbi.nlm.nih.gov/nuccore/" ]; fhir:Coding.code [ fhir:value "NM_000059.3" ]; fhir:Coding.display [ fhir:value "Homo sapiens BRCA2, DNA repair associated (BRCA2), mRNA" ] ] ]; fhir:Sequence.referenceSeq.windowStart [ fhir:value "101488058"^^xsd:integer ]; fhir:Sequence.referenceSeq.windowEnd [ fhir:value "101499444"^^xsd:integer ] ]; fhir:Sequence.variant [ fhir:index 0; fhir:Sequence.variant.start [ fhir:value "32316186"^^xsd:integer ]; fhir:Sequence.variant.end [ fhir:value "32316187"^^xsd:integer ]; fhir:Sequence.variant.observedAllele [ fhir:value "A" ]; fhir:Sequence.variant.referenceAllele [ fhir:value "C" ] ] . <http://hl7.org/fhir/Patient/brcapat> a fhir:Patient . # - ontology header ------------------------------------------------------------ <http://hl7.org/fhir/Sequence/breastcancer.ttl> a owl:Ontology; owl:imports fhir:fhir.ttl; owl:versionIRI <http://build.fhir.org/Sequence/breastcancer.ttl> . # -------------------------------------------------------------------------------------
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.