This HTML5 document contains 24 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_0111051
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_2218 n2:DOID_0050737 _:vb50944129 _:vb50944130
rdfs:label
platelet-type bleeding disorder 18
wdrs:describedby
n4:doid.owl
obo:id
DOID:0111051
obo:hasDbXref
ORDO:420566 ICD10CM:D69.1 OMIM:615888
obo:hasExactSynonym
bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency bleeding disorder due to CalDAG-GEFI deficiency BDPLT18
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A blood platelet disease characterized by autosomal recessive inheritance of mucocutaneous bleeding, prolonged and severe epistaxis, hematomas and bleeding after tooth extraction that has_material_basis_in homozygous mutation in the RASGRP2 gene on chromosome 11q13.
Subject Item
_:vb50944129
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n4:doid.owl
Subject Item
_:vb50944130
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000007
wdrs:describedby
n4:doid.owl