<http://purl.obolibrary.org/obo/DOID_12531>	<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_12531>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"von Willebrand disease"@en .
<http://purl.obolibrary.org/obo/DOID_12531>	<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_12531>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0042974"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"vascular pseudohemophilia"@en .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_1247> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"von Willebrand's-Jurgens' disease"@en .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:11093006"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"von Willebrand-Jrgens disease"@en .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D014842"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C68677"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:D68.0"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"vascular hemophilia"@en .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A blood coagulation disease that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:12531"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<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_12531>	<http://www.w3.org/2000/01/rdf-schema#label>	"von Willebrand's disease"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD9CM:286.4"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:7867"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"von Willebrand disorder"@en .
<http://purl.obolibrary.org/obo/DOID_12531>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .