<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal dominant deafness 1"@en .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.w3.org/2000/01/rdf-schema#label>	"autosomal dominant nonsyndromic deafness 1"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110541>	<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_0110541>	<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_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hereditary low frequency hearing loss 1"@en .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has_material_basis_in mutation in the DIAPH1 gene on chromosome 5q31."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110541"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050564> .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:124900"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Konigsmark syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:H90.3"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"DFNA1"@en .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"LFHL1"@en .
<http://purl.obolibrary.org/obo/DOID_0110541>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal dominant deafness 1, with or without thrombocytopenia"^^<http://www.w3.org/2001/XMLSchema#string> .