Release 5

This page is part of the FHIR Specification (v5.0.0: R5 - STU). This is the current published version in it's permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

Example CodeSystem/genomicstudy-changetype (Turtle)

Clinical Genomics Work GroupMaturity Level: N/AStandards Status: Informative

Raw Turtle (+ also see Turtle/RDF Format Specification)

Definition for Code SystemGenomicStudyChangeType

@prefix fhir: <http://hl7.org/fhir/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .

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

[] a fhir:CodeSystem ;
  fhir:id [ fhir:v "genomicstudy-changetype"] ;
  fhir:meta [
     fhir:lastUpdated [ fhir:v "2023-03-25T23:21:02.749-05:00" ] ;
     fhir:profile ( [ fhir:v "http://hl7.org/fhir/StructureDefinition/shareablecodesystem" ] )
  ] ;
  fhir:text [
     fhir:status [ fhir:v "generated" ]
  ] ;
  fhir:extension ( [
     fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-wg" ] ;
     fhir:value [ fhir:v "cg" ]
  ] [
     fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-standards-status" ] ;
     fhir:value [ fhir:v "trial-use" ]
  ] [
     fhir:url [ fhir:v "http://hl7.org/fhir/StructureDefinition/structuredefinition-fmm" ] ;
     fhir:value [ fhir:v "1" ]
  ] ) ;
  fhir:url [ fhir:v "http://hl7.org/fhir/genomicstudy-changetype"], [ fhir:v "http://hl7.org/fhir/genomicstudy-changetype"] ;
  fhir:identifier ( [
     fhir:system [ fhir:v "urn:ietf:rfc:3986" ] ;
     fhir:value [ fhir:v "urn:oid:2.16.840.1.113883.4.642.4.1977" ]
  ] [
     fhir:system [ fhir:v "urn:ietf:rfc:3986" ] ;
     fhir:value [ fhir:v "urn:oid:2.16.840.1.113883.4.642.4.1977" ]
  ] ) ;
  fhir:version [ fhir:v "5.0.0"], [ fhir:v "5.0.0"] ;
  fhir:name [ fhir:v "GenomicStudyChangeType"], [ fhir:v "GenomicStudyChangeType"] ;
  fhir:title [ fhir:v "Genomic Study Change Type"], [ fhir:v "Genomic Study Change Type"] ;
  fhir:status [ fhir:v "active"], [ fhir:v "active"] ;
  fhir:experimental [ fhir:v "true"], [ fhir:v "true"] ;
  fhir:date [ fhir:v "2022-08-17T15:48:24-05:00"], [ fhir:v "2022-08-17T15:48:24-05:00"] ;
  fhir:publisher [ fhir:v "HL7 (FHIR Project)"], [ fhir:v "HL7 (FHIR Project)"] ;
  fhir:contact ( [
     fhir:telecom ( [
       fhir:system [ fhir:v "url" ] ;
       fhir:value [ fhir:v "http://hl7.org/fhir" ]
     ] [
       fhir:system [ fhir:v "email" ] ;
       fhir:value [ fhir:v "fhir@lists.hl7.org" ]
     ] )
  ] [
     fhir:telecom ( [
       fhir:system [ fhir:v "url" ] ;
       fhir:value [ fhir:v "http://hl7.org/fhir" ]
     ] [
       fhir:system [ fhir:v "email" ] ;
       fhir:value [ fhir:v "fhir@lists.hl7.org" ]
     ] )
  ] ) ;
  fhir:description [ fhir:v "The change type relevant to GenomicStudy analysis."], [ fhir:v "The change type relevant to GenomicStudy analysis."] ;
  fhir:jurisdiction ( [
     fhir:coding ( [
       fhir:system [ fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm" ] ;
       fhir:code [ fhir:v "001" ] ;
       fhir:display [ fhir:v "World" ]
     ] )
  ] [
     fhir:coding ( [
       fhir:system [ fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm" ] ;
       fhir:code [ fhir:v "001" ] ;
       fhir:display [ fhir:v "World" ]
     ] )
  ] ) ;
  fhir:caseSensitive [ fhir:v "true"] ;
  fhir:valueSet [ fhir:v "http://hl7.org/fhir/ValueSet/genomicstudy-changetype"] ;
  fhir:content [ fhir:v "complete"] ;
  fhir:concept ( [
     fhir:code [ fhir:v "DNA" ] ;
     fhir:display [ fhir:v "DNA change" ] ;
     fhir:definition [ fhir:v "Change that involves Deoxyribonucleic acid (DNA) sequences." ]
  ] [
     fhir:code [ fhir:v "RNA" ] ;
     fhir:display [ fhir:v "RNA change" ] ;
     fhir:definition [ fhir:v "Change that involves Ribonucleic Acid (RNA) sequences." ]
  ] [
     fhir:code [ fhir:v "AA" ] ;
     fhir:display [ fhir:v "Protein/amino Acids change " ] ;
     fhir:definition [ fhir:v "Change that involves Amino Acid (AA) or protein sequences." ]
  ] [
     fhir:code [ fhir:v "CHR" ] ;
     fhir:display [ fhir:v "Chromosomal changes" ] ;
     fhir:definition [ fhir:v "Change that involves number or strcture of chromosomes." ]
  ] [
     fhir:code [ fhir:v "CNV" ] ;
     fhir:display [ fhir:v "Copy number variations" ] ;
     fhir:definition [ fhir:v "Change that involves copy number variations among various genomes." ]
  ] ) .

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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.