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DESCRIBE <http://purl.uniprot.org/SHA-384/DF94972BC1080829B204300A996007C084DF62548EF616509E74AEA96C7B0234364E98E6C31AF714BE88681B87987D2F>
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http://purl.uniprot.org/SHA-384/DF94972BC1080829B204300A996007C084DF62548EF616509E74AEA96C7B0234364E98E6C31AF714BE88681B87987D2F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/DF94972BC1080829B204300A996007C084DF62548EF616509E74AEA96C7B0234364E98E6C31AF714BE88681B87987D2F
http://www.w3.org/2000/01/rdf-schema#comment
"A novel missense mutation (F414C) KCNA1 identified in an Italian family affected by episodic ataxia type 1."
xsd:string
http://purl.uniprot.org/uniprot/#_C967E0C3603C77E49DDE34185A670BBDF8C8B606C294BE5B33D51803851453C2352B358D29B6307734FE04A59AAFD553
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/DF94972BC1080829B204300A996007C084DF62548EF616509E74AEA96C7B0234364E98E6C31AF714BE88681B87987D2F
http://purl.uniprot.org/uniprot/Q09470
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DF94972BC1080829B204300A996007C084DF62548EF616509E74AEA96C7B0234364E98E6C31AF714BE88681B87987D2F
http://purl.uniprot.org/uniprot/#_Q09470-mappedCitation-18926884
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DF94972BC1080829B204300A996007C084DF62548EF616509E74AEA96C7B0234364E98E6C31AF714BE88681B87987D2F