<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:4775"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndromic X-linked intellectual disability affects a person's height, muscles, skeleton, genitals, and appearance of the face."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Greig's syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q87.19"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"faciogenital dysplasia"@en .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C129720"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50954929	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50954929 .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:205809002"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50954929	<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_6683>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:305400"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_6683>	<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_6683>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C535331"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Aarskog-Scott syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:6683"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50954929	<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_6683>	<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_6683>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50954929	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000149> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0080012> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.w3.org/2000/01/rdf-schema#label>	"X-linked Aarskog syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0111824> .
<http://purl.obolibrary.org/obo/DOID_6683>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0175701"^^<http://www.w3.org/2001/XMLSchema#string> .