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Namespace Prefixes

Prefix	IRI
n5	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_0050958

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_1441

rdfs:label

spinocerebellar ataxia type 7

wdrs:describedby

n5:doid.owl

obo:id

DOID:0050958

obo:created_by

lschriml

obo:creation_date

2015-10-05T16:07:27Z

obo:hasDbXref

OMIM:164500

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene.