This HTML5 document contains 21 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n6https://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_0111047
rdf:type
owl:Class
rdfs:subClassOf
_:vb50944119 n2:DOID_2218 n2:DOID_0050736 _:vb50944120
rdfs:label
platelet-type bleeding disorder 14
wdrs:describedby
n6:doid.owl
obo:id
DOID:0111047
obo:hasDbXref
OMIM:614158
obo:hasExactSynonym
BDPLT14 thromboxane synthase deficiency
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A blood platelet disease characterized by autosomal dominant inheritance of defective platelet aggegation, epistaxis, ecchymoses, and prolonged bleeding times that has_material_basis_in mutation in the TBXAS1 gene on chromosome 7q34.
Subject Item
_:vb50944119
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n6:doid.owl
Subject Item
_:vb50944120
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000007
wdrs:describedby
n6:doid.owl