<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"X-linked McLeod syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:59306"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"McLeod neuroacanthocytosis syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"McLeod syndrome with or without chronic granulomatous disease"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:300842"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050765> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050735> .
_:vb50946094	<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_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C564038"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<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_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"McLeod type neuroacanthocytosis"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50946094	<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_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:234411007"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:10731"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.w3.org/2000/01/rdf-schema#label>	"McLeod syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50946094	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000936> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50946094 .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0398568"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0112107"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MLS"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50946094	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0112107>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A neuroacanthocytosis characterized by absence of red blood cell Kx antigen, weak expression of Kell red blood cell antigens, acanthocytosis, compensated hemolysis, and  involuntary movements that has_material_basis_in mutation in XK on chromosome Xp21.1."^^<http://www.w3.org/2001/XMLSchema#string> .