Genomics Reporting Implementation Guide, published by HL7 International / Clinical Genomics. This guide is not an authorized publication; it is the continuous build for version 3.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/genomics-reporting/ and changes regularly. See the Directory of published versions
@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 sct: <http://snomed.info/id/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
# - resource -------------------------------------------------------------------
a fhir:RiskAssessment ;
fhir:nodeRole fhir:treeRoot ;
fhir:id [ fhir:v "GenRiskDiabetesT2"] ; #
fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: RiskAssessment GenRiskDiabetesT2</b></p><a name=\"GenRiskDiabetesT2\"> </a><a name=\"hcGenRiskDiabetesT2\"> </a><a name=\"GenRiskDiabetesT2-en-US\"> </a><p><b>parent</b>: <a href=\"Observation-PolyGenicDiagnosticImpExample.html\">Observation Diagnostic Implication</a></p><p><b>status</b>: Final</p><p><b>subject</b>: <a href=\"Patient-CGPatientExample01.html\">Adam B. Everyman Male, DoB: 1951-01-20 ( Medical Record Number: m123 (use: usual, ))</a></p><p><b>basis</b>: </p><ul><li>Variant 1 (Identifier: <code>http://hospital.example.org</code>/11)</li><li>Variant 2 (Identifier: <code>http://hospital.example.org</code>/12)</li><li>Variant 3 (Identifier: <code>http://hospital.example.org</code>/13)</li><li>Variant 4 (Identifier: <code>http://hospital.example.org</code>/14)</li><li>Variant 5 (Identifier: <code>http://hospital.example.org</code>/15)</li><li>Variant 6 (Identifier: <code>http://hospital.example.org</code>/16)</li><li>Variant 7 (Identifier: <code>http://hospital.example.org</code>/17)</li></ul><blockquote><p><b>prediction</b></p><p><b>outcome</b>: <span title=\"Codes:{http://snomed.info/sct 44054006}\">Diabetes mellitus type 2 (disorder)</span></p><p><b>probability</b>: 0.26</p><p><b>qualitativeRisk</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/risk-probability low}\">Low likelihood</span></p><p><b>relativeRisk</b>: 1.05</p><p><b>when</b>: ?-53</p></blockquote><blockquote><p><b>prediction</b></p><p><b>outcome</b>: <span title=\"Codes:{http://snomed.info/sct 44054006}\">Diabetes mellitus type 2 (disorder)</span></p><p><b>probability</b>: 0.7</p><p><b>qualitativeRisk</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/risk-probability high}\">High likelihood</span></p><p><b>relativeRisk</b>: 2.69</p><p><b>when</b>: ?-65</p></blockquote></div>"
] ; #
fhir:parent [
fhir:reference [ fhir:v "Observation/PolyGenicDiagnosticImpExample" ]
] ; #
fhir:status [ fhir:v "final"] ; #
fhir:subject [
fhir:reference [ fhir:v "Patient/CGPatientExample01" ]
] ; #
fhir:basis ( [
fhir:identifier [
fhir:system [ fhir:v "http://hospital.example.org"^^xsd:anyURI ] ;
fhir:value [ fhir:v "11" ] ] ;
fhir:display [ fhir:v "Variant 1" ]
] [
fhir:identifier [
fhir:system [ fhir:v "http://hospital.example.org"^^xsd:anyURI ] ;
fhir:value [ fhir:v "12" ] ] ;
fhir:display [ fhir:v "Variant 2" ]
] [
fhir:identifier [
fhir:system [ fhir:v "http://hospital.example.org"^^xsd:anyURI ] ;
fhir:value [ fhir:v "13" ] ] ;
fhir:display [ fhir:v "Variant 3" ]
] [
fhir:identifier [
fhir:system [ fhir:v "http://hospital.example.org"^^xsd:anyURI ] ;
fhir:value [ fhir:v "14" ] ] ;
fhir:display [ fhir:v "Variant 4" ]
] [
fhir:identifier [
fhir:system [ fhir:v "http://hospital.example.org"^^xsd:anyURI ] ;
fhir:value [ fhir:v "15" ] ] ;
fhir:display [ fhir:v "Variant 5" ]
] [
fhir:identifier [
fhir:system [ fhir:v "http://hospital.example.org"^^xsd:anyURI ] ;
fhir:value [ fhir:v "16" ] ] ;
fhir:display [ fhir:v "Variant 6" ]
] [
fhir:identifier [
fhir:system [ fhir:v "http://hospital.example.org"^^xsd:anyURI ] ;
fhir:value [ fhir:v "17" ] ] ;
fhir:display [ fhir:v "Variant 7" ]
] ) ; #
fhir:prediction ( [
fhir:outcome [
( fhir:coding [
a sct:44054006 ;
fhir:system [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ] ;
fhir:code [ fhir:v "44054006" ] ;
fhir:display [ fhir:v "Diabetes mellitus type 2 (disorder)" ] ] ) ] ;
fhir:probability [ fhir:v "0.26"^^xsd:decimal ] ;
fhir:qualitativeRisk [
( fhir:coding [
fhir:system [ fhir:v "http://terminology.hl7.org/CodeSystem/risk-probability"^^xsd:anyURI ] ;
fhir:code [ fhir:v "low" ] ;
fhir:display [ fhir:v "Low likelihood" ] ] ) ] ;
fhir:relativeRisk [ fhir:v "1.05"^^xsd:decimal ] ;
fhir:when [
a fhir:Range ;
fhir:high [
fhir:value [ fhir:v "53"^^xsd:decimal ] ;
fhir:unit [ fhir:v "years" ] ;
fhir:system [ fhir:v "http://unitsofmeasure.org"^^xsd:anyURI ] ;
fhir:code [ fhir:v "a" ] ] ]
] [
fhir:outcome [
( fhir:coding [
a sct:44054006 ;
fhir:system [ fhir:v "http://snomed.info/sct"^^xsd:anyURI ] ;
fhir:code [ fhir:v "44054006" ] ;
fhir:display [ fhir:v "Diabetes mellitus type 2 (disorder)" ] ] ) ] ;
fhir:probability [ fhir:v "0.7"^^xsd:decimal ] ;
fhir:qualitativeRisk [
( fhir:coding [
fhir:system [ fhir:v "http://terminology.hl7.org/CodeSystem/risk-probability"^^xsd:anyURI ] ;
fhir:code [ fhir:v "high" ] ;
fhir:display [ fhir:v "High likelihood" ] ] ) ] ;
fhir:relativeRisk [ fhir:v "2.69"^^xsd:decimal ] ;
fhir:when [
a fhir:Range ;
fhir:high [
fhir:value [ fhir:v "65"^^xsd:decimal ] ;
fhir:unit [ fhir:v "years" ] ;
fhir:system [ fhir:v "http://unitsofmeasure.org"^^xsd:anyURI ] ;
fhir:code [ fhir:v "a" ] ] ]
] ) . #
IG © 2022+ HL7 International / Clinical Genomics. Package hl7.fhir.uv.genomics-reporting#3.0.0 based on FHIR 4.0.1. Generated 2024-11-19
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