This HTML5 document contains 17 embedded RDF statements represented using HTML+Microdata notation.

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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#
n8	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_0060573

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_12531

rdfs:label

von Willebrand's disease 1

wdrs:describedby

n6:doid.owl

obo:id

DOID:0060573

obo:hasDbXref

UMLS_CUI:C1264039 MESH:D056725 OMIM:193400 SNOMEDCT_US_2021_09_01:128106003 NCI:C131685

obo:hasExactSynonym

von Willebrand disease type 1 VWD1 von Willebrand disease type I VWD type 1

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:NCIthesaurus

n2:IAO_0000115

A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13.