_:vb50950628	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C131632"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50950628 .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.w3.org/2000/01/rdf-schema#label>	"factor X deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50950628	<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_2222>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0015519"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
_:vb50950628	<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_2222>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2222>	<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_2222>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50950628	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:2222"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:76642003"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_1247> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D005171"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Factor X deficiency"@en .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:6404"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_2222>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"disease, Stuart-Prower"@en .