<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.w3.org/2000/01/rdf-schema#label>	"platelet-type bleeding disorder 19"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111048"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:616176"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50944122	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:D69.4"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_2218> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:438207"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50944122	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"BDPLT19"@en .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A blood platelet disease characterized by autosomal recessive inheritance of epistaxis, spontaneous hematomas, severe thrombocytopenia, menorrhagia, ovarian cyst ruptures, and abnormal megakaryocytic clusters that has_material_basis_in homozygous mutation in the PRKACG gene on chromosome 9q21."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50944122 .
_:vb50944122	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50944122	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0111048>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"severe autosomal recessive macrothrombocytopenia"@en .