This HTML5 document contains 22 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n5https://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_0111055
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_2218 _:vb50944138 _:vb50944139 n2:DOID_0050736
rdfs:label
platelet-type bleeding disorder 20
wdrs:describedby
n5:doid.owl
obo:id
DOID:0111055
obo:hasDbXref
ORDO:466806 OMIM:616913
obo:hasExactSynonym
BDPLT20 autosomal dominant thrombocytopenia with platelet secretion defect
obo:hasOBONamespace
disease_ontology
n2: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.
Subject Item
_:vb50944138
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50944139
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000007
wdrs:describedby
n5:doid.owl