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DESCRIBE <http://purl.uniprot.org/SHA-384/6FAC17FA3FB48521B01C98C0371FB722AA973FC7DFD8B9584F2AA183DD2D181F13D294D7EBC39431B469C054C66DCC66>
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http://purl.uniprot.org/SHA-384/6FAC17FA3FB48521B01C98C0371FB722AA973FC7DFD8B9584F2AA183DD2D181F13D294D7EBC39431B469C054C66DCC66
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/6FAC17FA3FB48521B01C98C0371FB722AA973FC7DFD8B9584F2AA183DD2D181F13D294D7EBC39431B469C054C66DCC66
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); 4 new variants were found in exons of the ATP1A2 gene in sporadic hemiplegic migraine patients. It does not seem that ATP1A2 is a major gene in SHM."
xsd:string
http://purl.uniprot.org/uniprot/#_56BEB5145D8BDA013CEA307EA1FB2512FFBDF2BB319ACC001C9B6ABD0313BD1EE48E1CB4F07A8117044CDCB2F78A1CB9
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/6FAC17FA3FB48521B01C98C0371FB722AA973FC7DFD8B9584F2AA183DD2D181F13D294D7EBC39431B469C054C66DCC66
http://purl.uniprot.org/uniprot/B3KW93
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6FAC17FA3FB48521B01C98C0371FB722AA973FC7DFD8B9584F2AA183DD2D181F13D294D7EBC39431B469C054C66DCC66
http://purl.uniprot.org/uniprot/#_B3KW93-mappedCitation-18513263
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/6FAC17FA3FB48521B01C98C0371FB722AA973FC7DFD8B9584F2AA183DD2D181F13D294D7EBC39431B469C054C66DCC66