<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111612"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"SCABD"@en .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal recessive spinocerebellar ataxia-blindness-hearing loss syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:95433"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An autosomal recessive cerebellar ataxia characterized by spinocerebellar ataxia with optic and cochlear degeneration that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 6p23-p21."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050950> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.w3.org/2000/01/rdf-schema#label>	"autosomal recessive spinocerebellar ataxia 3"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal recessive spinocerebellar ataxia type 3"@en .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1849094"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:271250"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:9971"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111612>	<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_0111612>	<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_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"SCAR3"@en .
<http://purl.obolibrary.org/obo/DOID_0111612>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C537309"^^<http://www.w3.org/2001/XMLSchema#string> .