<http://purl.obolibrary.org/obo/DOID_0050993>	<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_0050993>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0050993"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050993>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:613855"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050993>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_963> .
<http://purl.obolibrary.org/obo/DOID_0050993>	<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_0050993>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An episodic ataxia that is characterized by dysarthria and vertigo, develops in early childhood, and has_material_basis_in autosomal dominant inheritance of mutation in the CACNB4 gene."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050993>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050993>	<http://www.geneontology.org/formats/oboInOwl#creation_date>	"2015-10-06T16:26:26Z"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050993>	<http://www.w3.org/2000/01/rdf-schema#label>	"episodic ataxia type 5"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050993>	<http://www.geneontology.org/formats/oboInOwl#created_by>	"lschriml"^^<http://www.w3.org/2001/XMLSchema#string> .