About: autosomal recessive spinocerebellar ataxia 7

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal recessive cerebellar ataxia
label	autosomal recessive spinocerebellar ataxia 7
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0080059
created_by	lschriml
creation_date	2015-10-07T14:55:44Z
database_cross_reference	GARD:12232 OMIM:609270
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	An autosomal recessive cerebellar ataxia that is characterized by onset of progressive gait difficulties, eye movement abnormalities, and dysarthria in the first or second decade of life and that has_material_basis_in compound heterozygous mutation in the TPP1 gene on chromosome 11p15.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50940312

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