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DESCRIBE <http://purl.uniprot.org/SHA-384/89C54B81E71368A52620195962BD9A162F5771F01C2A7C9BFE7C4ABA8A51E05E23E3B226449AE541E67AACCB89C3CD5D>
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http://purl.uniprot.org/SHA-384/89C54B81E71368A52620195962BD9A162F5771F01C2A7C9BFE7C4ABA8A51E05E23E3B226449AE541E67AACCB89C3CD5D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/89C54B81E71368A52620195962BD9A162F5771F01C2A7C9BFE7C4ABA8A51E05E23E3B226449AE541E67AACCB89C3CD5D
http://www.w3.org/2000/01/rdf-schema#comment
"Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2."
xsd:string
http://purl.uniprot.org/uniprot/#_44FAE644DB4D495993DBD00077F7463EE81F653B11145B8F442F88BEC91B50FF83DC948C6312FF7AF5183B002238888B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/89C54B81E71368A52620195962BD9A162F5771F01C2A7C9BFE7C4ABA8A51E05E23E3B226449AE541E67AACCB89C3CD5D
http://purl.uniprot.org/uniprot/B3KW93
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/89C54B81E71368A52620195962BD9A162F5771F01C2A7C9BFE7C4ABA8A51E05E23E3B226449AE541E67AACCB89C3CD5D
http://purl.uniprot.org/uniprot/#_B3KW93-mappedCitation-33711927
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/89C54B81E71368A52620195962BD9A162F5771F01C2A7C9BFE7C4ABA8A51E05E23E3B226449AE541E67AACCB89C3CD5D