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DESCRIBE <http://purl.uniprot.org/SHA-384/0AEC47EA7EF7BEEB8936C72EF50BBD7DCA0AA485734F20E90D39144AA4BAB4F9F021F6EEF6843C7272163190B195CF0A>
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http://purl.uniprot.org/SHA-384/0AEC47EA7EF7BEEB8936C72EF50BBD7DCA0AA485734F20E90D39144AA4BAB4F9F021F6EEF6843C7272163190B195CF0A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/0AEC47EA7EF7BEEB8936C72EF50BBD7DCA0AA485734F20E90D39144AA4BAB4F9F021F6EEF6843C7272163190B195CF0A
http://www.w3.org/2000/01/rdf-schema#comment
"We report on a family with ataxia type 6 (SCA6) showing peculiar oculomotor symptoms. They carried the identical mutation (the number of expanded CAG repeat 24) in the CACNA1A gene."
xsd:string
http://purl.uniprot.org/uniprot/#_96D08E4F69B9BF940A483B88235880CB278E56F45BD5DEACEDBCBF785F31EC058BF682355856AAE060EA3766960B2DDF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/0AEC47EA7EF7BEEB8936C72EF50BBD7DCA0AA485734F20E90D39144AA4BAB4F9F021F6EEF6843C7272163190B195CF0A
http://purl.uniprot.org/uniprot/O00555
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0AEC47EA7EF7BEEB8936C72EF50BBD7DCA0AA485734F20E90D39144AA4BAB4F9F021F6EEF6843C7272163190B195CF0A
http://purl.uniprot.org/uniprot/#_O00555-mappedCitation-14534930
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/0AEC47EA7EF7BEEB8936C72EF50BBD7DCA0AA485734F20E90D39144AA4BAB4F9F021F6EEF6843C7272163190B195CF0A