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

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Namespace Prefixes

PrefixIRI
n4https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0060691
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_2218 _:vb50939210 _:vb50939211 n2:DOID_0050736
rdfs:label
platelet-type bleeding disorder 16
wdrs:describedby
n4:doid.owl
obo:id
DOID:0060691
obo:hasDbXref
ORDO:140957 ICD10CM:D69.4 OMIM:187800
obo:hasExactSynonym
autosomal dominant thrombasthenia of Glanzmann and Naegeli autosomal dominant Glanzmann thrombasthenia
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A blood platelet disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has material basis_in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32.
Subject Item
_:vb50939210
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n4:doid.owl
Subject Item
_:vb50939211
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000007
wdrs:describedby
n4:doid.owl