_:vb50939451	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
<http://purl.obolibrary.org/obo/DOID_0060819>	<http://www.w3.org/2000/01/rdf-schema#label>	"syndromic X-linked intellectual disability Chudley-Schwartz type"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060819>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060819"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50939451	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0000363> .
<http://purl.obolibrary.org/obo/DOID_0060819>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"mental retardation, X-linked, syndromic, Chudley-Schwartz type"@en .
<http://purl.obolibrary.org/obo/DOID_0060819>	<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_0060819>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060819>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50939451 .
<http://purl.obolibrary.org/obo/DOID_0060819>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:300861"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060819>	<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_0060819>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndromic X-linked intellectual disability characterized by moderate intellectual disability, seizures, dysmorphic facial features and in some older patients slowly progressive unsteady gait and progressive weakness that has_material_basis_in variation in the chromosomal region Xq21.33-q23."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060819>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MRXSCS"@en .
<http://purl.obolibrary.org/obo/DOID_0060819>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"X-linked mental retardation with seizures, hypogammaglobinemia, and gait disturbance"@en .
_:vb50939451	<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_0060819>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060309> .
_:vb50939451	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .