This HTML5 document contains 23 embedded RDF statements represented using HTML+Microdata notation.

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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_0060692

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_2218 _:vb50939213 _:vb50939214 n2:DOID_0050737

rdfs:label

platelet-type bleeding disorder 8

wdrs:describedby

n7:doid.owl

obo:id

DOID:0060692

obo:hasDbXref

OMIM:609821 ORDO:36355 ICD10CM:D69.8

obo:hasExactSynonym

ADP platelet receptor P2Y12 defect P2Y12 defect

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

A blood platelet disease characterized by mild to moderate mucocutaneous bleeding and absence of adenosine phosphate induced platelet aggregation that has_material_basis_in homozygous or compound heterozygous mutation in the P2RY12 gene on chromosome 3q.

Subject Item

_:vb50939213

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000148

wdrs:describedby

n7:doid.owl

Subject Item

_:vb50939214

rdf:type

owl:Restriction

owl:onProperty

n2:RO_0002452

owl:someValuesFrom

n2:SYMP_0000007

wdrs:describedby

n7:doid.owl