About: platelet-type bleeding disorder 20

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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://b50944138 nodeID://b50944139
label	platelet-type bleeding disorder 20
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0111055
database_cross_reference	OMIM:616913 ORDO:466806
has_exact_synonym	BDPLT20 (en) autosomal dominant thrombocytopenia with platelet secretion defect (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A blood platelet disease characterized by autosomal dominant inheritance of increased bleeding tendency, thrombocytopenia, decreased platelet dense granules and ATP secretion, and impaired megakaryocyte maturation that has_material_basis_in heterozygous mutation in the SLFN14 gene on chromosome 17q12.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50944140

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