<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D005166"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.w3.org/2000/01/rdf-schema#label>	"factor V deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"deficiency, labile"@en .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50950610 .
_:vb50950610	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
_:vb50950610	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_1247> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Hereditary hypoproaccelerinaemia"@en .
_:vb50950610	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:227400"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:2216"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0015499"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Proaccelerin deficiency"@en .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50950610	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Labile factor deficiency"@en .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:2237"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:191284007"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C98938"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2216>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:D68.2"^^<http://www.w3.org/2001/XMLSchema#string> .