Evidence Based Medicine on FHIR Implementation Guide, published by HL7 International / Clinical Decision Support. This guide is not an authorized publication; it is the continuous build for version 1.0.0-ballot3 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/ebm/ and changes regularly. See the Directory of published versions
: Correlation of single nucleotide variant (SNV) and copy number variant (CNV) profiles with treatment response (NCT05327010)
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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 -------------------------------------------------------------------
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fhir:lastUpdated [ fhir:v "2026-07-27T13:49:52.712Z"^^xsd:dateTime ] ;
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fhir:l <http://hl7.org/fhir/uv/ebm/StructureDefinition/variable-definition>
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] ; #
fhir:language [ fhir:v "en"] ; #
fhir:text [
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fhir:div [ fhir:v "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: EvidenceVariable 583777</b></p><a name=\"583777\"> </a><a name=\"hc583777\"> </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\">version: 2; Last updated: 2026-07-27 13:49:52+0000</p><p style=\"margin-bottom: 0px\">Profile: <a href=\"StructureDefinition-variable-definition.html\">VariableDefinition</a></p></div><p><b>ArtifactPublicationStatus</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/cited-artifact-status-type active}\">Active</span></p><p><b>url</b>: <a href=\"https://fevir.net/resources/EvidenceVariable/583777\">https://fevir.net/resources/EvidenceVariable/583777</a></p><p><b>identifier</b>: FEvIR Object Identifier/583777, FEvIR Linking Identifier/NCT05327010-otherOutcome-1</p><p><b>name</b>: Correlation_of_single_nucleotide_variant_SNV_and_copy_number_variant_CNV_profiles_with_treatment_response_NCT05327010</p><p><b>title</b>: Correlation of single nucleotide variant (SNV) and copy number variant (CNV) profiles with treatment response (NCT05327010)</p><p><b>citeAs</b>: </p><div><p>Correlation of single nucleotide variant (SNV) and copy number variant (CNV) profiles with treatment response (NCT05327010) [Database Entry: FHIR EvidenceVariable Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 583777. Revised 2026-07-27. Available at: https://fevir.net/resources/EvidenceVariable/583777. Computable resource at: https://fevir.net/resources/EvidenceVariable/583777#json.</p>\n</div><p><b>status</b>: Active</p><p><b>author</b>: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter: </p><p><b>publisher</b>: Computable Publishing LLC</p><p><b>contact</b>: <a href=\"mailto:support@computablepublishing.com\">support@computablepublishing.com</a></p><p><b>description</b>: </p><div><p>Whole exome sequencing conducted on pre-treatment biopsy and at progression to correlate SNV and CNV profiles with treatment response.</p>\n</div><p><b>copyright</b>: </p><div><p>Copyright the Authors else Computable Publishing LLC. Noncommercial use permitted with CC BY-NC-SA 4.0 (https://creativecommons.org/licenses/by-nc-sa/4.0/). Commercial use permitted as agreed in Terms of Use (https://fevir.net/termsofuse).</p>\n</div><h3>Definitions</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Concept</b></td></tr><tr><td style=\"display: none\">*</td><td><span title=\"Codes:\">Correlation of single nucleotide variant (SNV) and copy number variant (CNV) profiles with treatment response Whole exome sequencing conducted on pre-treatment biopsy and at progression to correlate SNV and CNV profiles with treatment response.</span></td></tr></table><p><b>handling</b>: <span title=\"Codes:{https://fevir.net/resources/CodeSystem/179423 evidence-variable-handling-not-specified}\">Evidence variable handling not specified</span></p><h3>Timings</h3><table class=\"grid\"><tr><td style=\"display: none\">-</td><td><b>Text</b></td></tr><tr><td style=\"display: none\">*</td><td>Up to 2 years</td></tr></table></div>"^^rdf:XMLLiteral ]
] ; #
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fhir:name [ fhir:v "Correlation_of_single_nucleotide_variant_SNV_and_copy_number_variant_CNV_profiles_with_treatment_response_NCT05327010"] ; #
fhir:title [ fhir:v "Correlation of single nucleotide variant (SNV) and copy number variant (CNV) profiles with treatment response (NCT05327010)"] ; #
fhir:citeAs [ fhir:v "Correlation of single nucleotide variant (SNV) and copy number variant (CNV) profiles with treatment response (NCT05327010) [Database Entry: FHIR EvidenceVariable Resource]. Contributors: Computable Publishing®: ClinicalTrials.gov-to-FEvIR Converter [Authors/Creators]. In: Fast Evidence Interoperability Resources (FEvIR) Platform, FOI 583777. Revised 2026-07-27. Available at: https://fevir.net/resources/EvidenceVariable/583777. Computable resource at: https://fevir.net/resources/EvidenceVariable/583777#json."] ; #
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fhir:description [ fhir:v "Whole exome sequencing conducted on pre-treatment biopsy and at progression to correlate SNV and CNV profiles with treatment response."] ; #
fhir:copyright [ fhir:v "Copyright the Authors else Computable Publishing LLC. Noncommercial use permitted with CC BY-NC-SA 4.0 (https://creativecommons.org/licenses/by-nc-sa/4.0/). Commercial use permitted as agreed in Terms of Use (https://fevir.net/termsofuse)."] ; #
fhir:definition [
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fhir:timing [
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