This page is part of the Adverse Event Clinical Research (v1.0.1: STU 1) based on FHIR (HL7® FHIR® Standard) v5.0.0. This is the current published version. For a full list of available versions, see the Directory of published versions
: ClinicalTrialSubject5 - TTL Representation
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@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 xsd: <http://www.w3.org/2001/XMLSchema#> .
# - resource -------------------------------------------------------------------
a fhir:Patient ;
fhir:nodeRole fhir:treeRoot ;
fhir:id [ fhir:v "ClinicalTrialSubject5"] ; #
fhir:text [
fhir:status [ fhir:v "generated" ] ;
fhir:div "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p style=\"border: 1px #661aff solid; background-color: #e6e6ff; padding: 10px;\"><b>Subject 5 Clinical Trial </b> (no stated gender), DoB Unknown</p><hr/></div>"
] ; #
fhir:name ( [
fhir:family [ fhir:v "Clinical Trial" ] ;
( fhir:given [ fhir:v "Subject 5" ] )
] ) . #