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http://purl.uniprot.org/diseases/2959http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/2959http://www.w3.org/2000/01/rdf-schema#comment"A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR10 is characterized by onset in the teenage or young adult years of gait and limb ataxia, dysarthria, and nystagmus associated with marked cerebellar atrophy on brain imaging."xsd:string
http://purl.uniprot.org/diseases/2959http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/613728
http://purl.uniprot.org/diseases/2959http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/523
http://purl.uniprot.org/diseases/2959http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D002524
http://purl.uniprot.org/diseases/2959http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D013132
http://purl.uniprot.org/diseases/2959http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C3150998
http://purl.uniprot.org/diseases/2959http://www.w3.org/2004/02/skos/core#prefLabel"Spinocerebellar ataxia, autosomal recessive, 10"xsd:string
http://purl.uniprot.org/diseases/2959http://purl.uniprot.org/core/mnemonic"SCAR10"xsd:string
http://purl.uniprot.org/uniprot/Q9NW15#SIP87DF656D111BC34Fhttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/2959
http://purl.uniprot.org/annotation/VAR_064888http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/2959
http://purl.uniprot.org/uniprot/#_50AB0F75DA39C555_up.disease_72E920BE9D98448Fhttp://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/2959