<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:4684"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C126329"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.w3.org/2000/01/rdf-schema#label>	"retinitis pigmentosa-deafness syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50943740	<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_0110829>	<http://www.w3.org/2000/01/rdf-schema#comment>	"Orphanet has this as part of USH3, reference listed refers to symptoms being almost identical to USH3 but inheritance pattern is different. I made this a child of Usher Syndrome but not USH3 - smb."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110829"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50943740	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:500004"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1568248"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50943740	<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_0110829>	<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_0110829>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An Usher syndrome characterized by retinitis pigmentosa and onset of sensorineural hearing impairment in the teens that has_material_basis_in mutation in the MTTS2 gene in the mitochondrial genome."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50943740	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<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_0110829>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050439> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:1010610007"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50943740 .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D052245"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110829>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:231183"^^<http://www.w3.org/2001/XMLSchema#string> .