<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_2218> .
_:vb50950619	<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_2219>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [LS]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"platelet glycoprotein IIb-IIIa deficiency"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"deficiency of platelet fibrinogen receptor"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"deficiency of GP IIb-IIIa complex"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"thrombasthenia of Glanzmann and Naegeli"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"platelet-type bleeding disorder 2"@en .
_:vb50950619	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/CL_0000233> .
_:vb50950619	<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_2219>	<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_2219>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D013915"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Thrombocytasthenia"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Glycoprotein IIb/IIIa defect"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Glanzmann thrombasthenia"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<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_2219>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:32942005"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:D69.1"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0040015"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:849"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:2219"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:2478"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:273800"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C61249"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50950619	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0004026> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"deficiency of glycoprotein complex IIb-IIIa"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"BDPLT2"@en .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50950619 .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://www.w3.org/2000/01/rdf-schema#label>	"Glanzmann's thrombasthenia"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2219>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A blood coagulation disease characterized by autosomal recessive inheritance of failure of platelet aggregation and absent or diminished clot retraction that has material_basis_in mutation in the ITGA2B or ITGB3 genes on chromosome 17q21.32."^^<http://www.w3.org/2001/XMLSchema#string> .