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DESCRIBE <http://purl.uniprot.org/SHA-384/953D539B810B82F6D45EB1D49FFB4357A9C8CB6CC9C22C090F128B91FC939922A66036757BED0CD5C1C5862A72DD9604>
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http://purl.uniprot.org/SHA-384/953D539B810B82F6D45EB1D49FFB4357A9C8CB6CC9C22C090F128B91FC939922A66036757BED0CD5C1C5862A72DD9604
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/953D539B810B82F6D45EB1D49FFB4357A9C8CB6CC9C22C090F128B91FC939922A66036757BED0CD5C1C5862A72DD9604
http://www.w3.org/2000/01/rdf-schema#comment
"A heterozygous nt 5404 T>C substitution in exon 33 was associated with co-occurrence of familial hemiplegic migraine and childhood epilepsy."
xsd:string
http://purl.uniprot.org/uniprot/#_A0CBF29C50F019F57F7C5E6BD72C8C5176D3431AA0F5B0A0C305DB9755E142A52C2F2854EAFAC33A79BA9FA224199042
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/953D539B810B82F6D45EB1D49FFB4357A9C8CB6CC9C22C090F128B91FC939922A66036757BED0CD5C1C5862A72DD9604
http://purl.uniprot.org/uniprot/O00555
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/953D539B810B82F6D45EB1D49FFB4357A9C8CB6CC9C22C090F128B91FC939922A66036757BED0CD5C1C5862A72DD9604
http://purl.uniprot.org/uniprot/#_O00555-mappedCitation-15452324
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/953D539B810B82F6D45EB1D49FFB4357A9C8CB6CC9C22C090F128B91FC939922A66036757BED0CD5C1C5862A72DD9604