<http://purl.obolibrary.org/obo/DOID_0111739>	<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_0111739>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"DFN2"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111739>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"DFNX1"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111739>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111739"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111739>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:304500"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111739>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"X-linked sensorineural congenital deafness 2"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111739>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An X-linked nonsyndromic deafness characterized by congenital profound sensorineural hearing loss in males and mild to moderate high-frequency hearing loss in heterozygous females that has_material_basis_in mutation in PRPS1 on chromosome Xq22.3."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111739>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111739>	<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_0111739>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050566> .
<http://purl.obolibrary.org/obo/DOID_0111739>	<http://www.w3.org/2000/01/rdf-schema#label>	"X-linked deafness 1"^^<http://www.w3.org/2001/XMLSchema#string> .