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Namespace Prefixes

Prefix	IRI
n6	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n7	http://purl.obolibrary.org/obo/doid#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_12531

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_1247

rdfs:label

von Willebrand's disease

rdfs:comment

OMIM mapping confirmed by DO. [SN].

wdrs:describedby

n6:doid.owl

obo:id

DOID:12531

obo:hasDbXref

UMLS_CUI:C0042974 SNOMEDCT_US_2021_09_01:11093006 MESH:D014842 NCI:C68677 ICD10CM:D68.0 ICD9CM:286.4 GARD:7867

obo:hasExactSynonym

von Willebrand disease vascular pseudohemophilia von Willebrand's-Jurgens' disease von Willebrand-Jrgens disease vascular hemophilia von Willebrand disorder

obo:hasOBONamespace

disease_ontology

obo:inSubset

n7:NCIthesaurus

n2: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.