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DESCRIBE <http://purl.uniprot.org/SHA-384/F781C81E40B93FECE69BF45C9D72A38F2EF6FFEF6BA1366B92A555CC2C860CFC2BC2DD6A5F1F84342E4624B4563AC03B>
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http://purl.uniprot.org/SHA-384/F781C81E40B93FECE69BF45C9D72A38F2EF6FFEF6BA1366B92A555CC2C860CFC2BC2DD6A5F1F84342E4624B4563AC03B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F781C81E40B93FECE69BF45C9D72A38F2EF6FFEF6BA1366B92A555CC2C860CFC2BC2DD6A5F1F84342E4624B4563AC03B
http://www.w3.org/2000/01/rdf-schema#comment
"Genetic testing in both patients reveals previously unidentified mutations in the CLCN1 gene specific to Myotonia Congenita"
xsd:string
http://purl.uniprot.org/uniprot/#_5ECC621A17319F64A69551791560C67AE8E91D88E56ABC0B6D6269206DB6FFC31EFD65FAE1C5A8D71553B29F28B54D55
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F781C81E40B93FECE69BF45C9D72A38F2EF6FFEF6BA1366B92A555CC2C860CFC2BC2DD6A5F1F84342E4624B4563AC03B
http://purl.uniprot.org/uniprot/P35523
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F781C81E40B93FECE69BF45C9D72A38F2EF6FFEF6BA1366B92A555CC2C860CFC2BC2DD6A5F1F84342E4624B4563AC03B
http://purl.uniprot.org/uniprot/#_P35523-mappedCitation-23483815
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F781C81E40B93FECE69BF45C9D72A38F2EF6FFEF6BA1366B92A555CC2C860CFC2BC2DD6A5F1F84342E4624B4563AC03B