MII IG Kerndatensatz-Modul Molekulares Tumorboard, published by Medizininformatik-Initiative. This guide is not an authorized publication; it is the continuous build for version 2026.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/medizininformatik-initiative/kerndatensatzmodul-molekulares-tumorboard/ and changes regularly. See the Directory of published versions
: MII CS Genomic Analysis Method Type - 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 "mii-cs-mtb-genomic-analysis-method-type"] ; #
fhir:language [ fhir:v "de-DE"] ; #
fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div [ fhir:v "<div xml:lang=\"de-DE\" xmlns=\"http://www.w3.org/1999/xhtml\" lang=\"de-DE\"><p class=\"res-header-id\"><b>Generated Narrative: CodeSystem mii-cs-mtb-genomic-analysis-method-type</b></p><a name=\"mii-cs-mtb-genomic-analysis-method-type\"> </a><a name=\"hcmii-cs-mtb-genomic-analysis-method-type\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\">Language: de-DE</p></div><p>This case-sensitive code system <code>https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-genomic-analysis-method-type</code> defines the 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\">tngs<a name=\"mii-cs-mtb-genomic-analysis-method-type-tngs\"> </a></td><td>Targeted NGS</td></tr><tr><td style=\"white-space:nowrap\">gene-panel<a name=\"mii-cs-mtb-genomic-analysis-method-type-gene-panel\"> </a></td><td>Genpanel</td></tr><tr><td style=\"white-space:nowrap\">fusion-detection-panel<a name=\"mii-cs-mtb-genomic-analysis-method-type-fusion-detection-panel\"> </a></td><td>Fusions-Detektions-Panel</td></tr><tr><td style=\"white-space:nowrap\">whole-genom-sequencing<a name=\"mii-cs-mtb-genomic-analysis-method-type-whole-genom-sequencing\"> </a></td><td>Whole Genom Sequencing (WGS)</td></tr><tr><td style=\"white-space:nowrap\">whole-exom-sequencing<a name=\"mii-cs-mtb-genomic-analysis-method-type-whole-exom-sequencing\"> </a></td><td>Whole Exom Sequencing (WES)</td></tr><tr><td style=\"white-space:nowrap\">rnaseq-transcriptomics<a name=\"mii-cs-mtb-genomic-analysis-method-type-rnaseq-transcriptomics\"> </a></td><td>RNA Sequencing (RNA-Seq)</td></tr></table></div>"^^rdf:XMLLiteral ]
] ; #
fhir:url [
fhir:v "https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-genomic-analysis-method-type"^^xsd:anyURI ;
fhir:l <https://www.medizininformatik-initiative.de/fhir/ext/modul-mtb/CodeSystem/mii-cs-mtb-genomic-analysis-method-type>
] ; #
fhir:version [ fhir:v "2026.0.0"] ; #
fhir:name [ fhir:v "MII_CS_MTB_Genomic_Analysis_Method_Type"] ; #
fhir:title [ fhir:v "MII CS Genomic Analysis Method Type"] ; #
fhir:status [ fhir:v "active"] ; #
fhir:experimental [ fhir:v false] ; #
fhir:date [ fhir:v "2026-02-09T10:07:17+00:00"^^xsd:dateTime] ; #
fhir:publisher [ fhir:v "Medizininformatik-Initiative"] ; #
fhir:contact ( [
fhir:name [ fhir:v "Medizininformatik-Initiative" ] ;
( fhir:telecom [
fhir:system [ fhir:v "url" ] ;
fhir:value [ fhir:v "https://www.medizininformatik-initiative.de" ] ] )
] ) ; #
fhir:description [ fhir:v "Codesystem, welches die verwendeten NGS-Methodiken gemäß dnpm-Kodierung high-level auflistet"] ; #
fhir:jurisdiction ( [
( fhir:coding [
fhir:system [
fhir:v "http://unstats.un.org/unsd/methods/m49/m49.htm"^^xsd:anyURI ;
fhir:l <http://unstats.un.org/unsd/methods/m49/m49.htm> ] ;
fhir:code [ fhir:v "276" ] ] )
] ) ; #
fhir:caseSensitive [ fhir:v true] ; #
fhir:content [ fhir:v "complete"] ; #
fhir:count [ fhir:v "6"^^xsd:nonNegativeInteger] ; #
fhir:concept ( [
fhir:code [ fhir:v "tngs" ] ;
fhir:display [ fhir:v "Targeted NGS" ]
] [
fhir:code [ fhir:v "gene-panel" ] ;
fhir:display [ fhir:v "Genpanel" ]
] [
fhir:code [ fhir:v "fusion-detection-panel" ] ;
fhir:display [ fhir:v "Fusions-Detektions-Panel" ]
] [
fhir:code [ fhir:v "whole-genom-sequencing" ] ;
fhir:display [ fhir:v "Whole Genom Sequencing (WGS)" ]
] [
fhir:code [ fhir:v "whole-exom-sequencing" ] ;
fhir:display [ fhir:v "Whole Exom Sequencing (WES)" ]
] [
fhir:code [ fhir:v "rnaseq-transcriptomics" ] ;
fhir:display [ fhir:v "RNA Sequencing (RNA-Seq)" ]
] ) . #