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DESCRIBE <http://purl.uniprot.org/SHA-384/4A6BE1B44F3D4010A42517070BF9C647F77CC0E176FC4988251EB35A6DEC04E057B5AA052FCD22573D07BE38E8071F05>
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http://purl.uniprot.org/SHA-384/4A6BE1B44F3D4010A42517070BF9C647F77CC0E176FC4988251EB35A6DEC04E057B5AA052FCD22573D07BE38E8071F05
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4A6BE1B44F3D4010A42517070BF9C647F77CC0E176FC4988251EB35A6DEC04E057B5AA052FCD22573D07BE38E8071F05
http://www.w3.org/2000/01/rdf-schema#comment
"Different phenotypes of neurological diseases including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism caused by de novo ATP1A3 mutation in a family."
xsd:string
http://purl.uniprot.org/uniprot/#_C0C4F31C698FDD16F0971CC96DDA252D1FF9F85E4410537686BFF8BB7CA64C8C2840A4BE059A20BF2AE4FE62020590FF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4A6BE1B44F3D4010A42517070BF9C647F77CC0E176FC4988251EB35A6DEC04E057B5AA052FCD22573D07BE38E8071F05
http://purl.uniprot.org/uniprot/B7Z1Q9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4A6BE1B44F3D4010A42517070BF9C647F77CC0E176FC4988251EB35A6DEC04E057B5AA052FCD22573D07BE38E8071F05
http://purl.uniprot.org/uniprot/#_B7Z1Q9-mappedCitation-34783933
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4A6BE1B44F3D4010A42517070BF9C647F77CC0E176FC4988251EB35A6DEC04E057B5AA052FCD22573D07BE38E8071F05