NHS North West Genomics, published by NHS North West Genomics. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/nw-gmsa/nw-gmsa.github.com/ and changes regularly. See the Directory of published versions
: iGene Test Codes - TTL Representation
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@prefix fhir: <http://hl7.org/fhir/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
# - resource -------------------------------------------------------------------
a fhir:CodeSystem ;
fhir:nodeRole fhir:treeRoot ;
fhir:id [ fhir:v "IGEAP"] ; #
fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div [ fhir:v "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: CodeSystem IGEAP</b></p><a name=\"IGEAP\"> </a><a name=\"hcIGEAP\"> </a><p>This case-sensitive code system <code>https://fhir.nwgenomics.nhs.uk/CodeSystem/IGEAP</code> provides <b>a fragment</b> that includes following codes:</p><table class=\"codes\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td style=\"white-space:nowrap\">SANGER<a name=\"IGEAP-SANGER\"> </a></td><td>TEST: Sanger Sequencing</td></tr><tr><td style=\"white-space:nowrap\">R125_Cardiology<a name=\"IGEAP-R125_Cardiology\"> </a></td><td>PANEL: R125.1, R125.2 - Thoracic aortic aneurysm and dissection v1.2</td></tr><tr><td style=\"white-space:nowrap\">CCP19v1_R112<a name=\"IGEAP-CCP19v1_R112\"> </a></td><td>PANEL: R112.1 - Factor II deficiency v1.0</td></tr></table></div>"^^rdf:XMLLiteral ]
] ; #
fhir:url [
fhir:v "https://fhir.nwgenomics.nhs.uk/CodeSystem/IGEAP"^^xsd:anyURI ;
fhir:l <https://fhir.nwgenomics.nhs.uk/CodeSystem/IGEAP>
] ; #
fhir:version [ fhir:v "0.1.0"] ; #
fhir:name [ fhir:v "IGEAP"] ; #
fhir:title [ fhir:v "iGene Test Codes"] ; #
fhir:status [ fhir:v "active"] ; #
fhir:experimental [ fhir:v false] ; #
fhir:date [ fhir:v "2026-02-05"^^xsd:date] ; #
fhir:publisher [ fhir:v "NHS North West Genomics"] ; #
fhir:contact ( [
( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "https://www.nwgenomics.nhs.uk/contact-us" ] ] )
] ) ; #
fhir:description [ fhir:v "iGene Test Codes"] ; #
fhir:jurisdiction ( [
( fhir:coding [
fhir:system [
fhir:v "urn:iso:std:iso:3166"^^xsd:anyURI ;
fhir:l <urn:iso:std:iso:3166> ] ;
fhir:code [ fhir:v "GB" ] ;
fhir:display [ fhir:v "United Kingdom of Great Britain and Northern Ireland" ] ] )
] ) ; #
fhir:caseSensitive [ fhir:v true] ; #
fhir:content [ fhir:v "fragment"] ; #
fhir:concept ( [
fhir:code [ fhir:v "SANGER" ] ;
fhir:display [ fhir:v "TEST: Sanger Sequencing" ]
] [
fhir:code [ fhir:v "R125_Cardiology" ] ;
fhir:display [ fhir:v "PANEL: R125.1, R125.2 - Thoracic aortic aneurysm and dissection v1.2" ]
] [
fhir:code [ fhir:v "CCP19v1_R112" ] ;
fhir:display [ fhir:v "PANEL: R112.1 - Factor II deficiency v1.0" ]
] ) . #
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