About: platelet-type bleeding disorder 12

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease blood platelet disease nodeID://b50944146 nodeID://b50944147
label	platelet-type bleeding disorder 12
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0111058
database_cross_reference	OMIM:605735
has_exact_synonym	platelet prostaglandin-endoperoxide synthase 1 deficiency (en) BDPLT12 (en) PGHS1 deficiency (en) platelet COX1 deficiency (en) platelet cyclooxygenase 1 deficiency (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A blood platelet disease characterized by autosomal dominant inheritance of mildly increased bleeding, platelet aggregation defect, and impaired conversion of arachidonic acid to thromboxane A2 in platelets due to deficiency in PTGS1 activity.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50944148

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