About: autosomal recessive spinocerebellar ataxia 2

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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 2
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0080061
created_by	lschriml
creation_date	2015-10-07T14:55:44Z
database_cross_reference	OMIM:213200
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	An autosomal recessive cerebellar ataxia that is characterized by juvenile onset of progressive cerebellar ataxia, axonal sensorimotor peripheral neuropathy, and increased serum alpha-fetoprotein, and has_material_basis_in homozygous or compound heterozygous mutation in the senataxin gene on chromosome 9q34.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50940314

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