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DESCRIBE <http://purl.uniprot.org/SHA-384/6A6B7F7779B032C5EE9CFFA87DA84A83B178A9DC1F32FDBD54AFD792F7808B2DC5BB2A63D2962BAA616E6ABB5C87B66A>
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http://purl.uniprot.org/SHA-384/6A6B7F7779B032C5EE9CFFA87DA84A83B178A9DC1F32FDBD54AFD792F7808B2DC5BB2A63D2962BAA616E6ABB5C87B66A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/6A6B7F7779B032C5EE9CFFA87DA84A83B178A9DC1F32FDBD54AFD792F7808B2DC5BB2A63D2962BAA616E6ABB5C87B66A
http://www.w3.org/2000/01/rdf-schema#comment
"SCA14 a novel mutation in the PRKCG gene was found in two families in Norway with autosomal dominant cerebellar ataxia."
xsd:string
http://purl.uniprot.org/uniprot/#_39D3F0D32532DFCE927F6E9C8AC2BB77730DD9A85DF20E9A5A6797069C410FFD7D0277BE8D476B7348D70B5683EA6598
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/6A6B7F7779B032C5EE9CFFA87DA84A83B178A9DC1F32FDBD54AFD792F7808B2DC5BB2A63D2962BAA616E6ABB5C87B66A
http://purl.uniprot.org/uniprot/B2R5T1
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6A6B7F7779B032C5EE9CFFA87DA84A83B178A9DC1F32FDBD54AFD792F7808B2DC5BB2A63D2962BAA616E6ABB5C87B66A
http://purl.uniprot.org/uniprot/#_B2R5T1-mappedCitation-21434874
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6A6B7F7779B032C5EE9CFFA87DA84A83B178A9DC1F32FDBD54AFD792F7808B2DC5BB2A63D2962BAA616E6ABB5C87B66A