SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
n7 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#
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_0111146
rdf:type
owl:Class
rdfs:subClassOf
_:vb50944308
n2:DOID_1247
rdfs:label
acquired von Willebrand syndrome
wdrs:describedby
n7:doid.owl
obo:id
DOID:0111146
obo:hasDbXref
MEDDRA:10069495
ORDO:99147
SNOMEDCT_US_2021_09_01:234451005
GARD:5573
UMLS_CUI:C0272362
obo:hasExactSynonym
AVWS
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A blood coagulation disease characterized by development of a defect in clotting in the absence of previous bleeding symptoms, negative familial history, and occurrence in a relatively older age. Typically this develops secondarily to other disorders, such as lymphoproliferative, myeloproliferative, cardiovascular and autoimmune disorders.
Subject Item _:vb50944308
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000007
wdrs:describedby
n7:doid.owl