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DESCRIBE <http://purl.uniprot.org/SHA-384/FCC10C469E8235527C728904D72323BC790D12AC15BD476BBE6F2487832F1115D2BB9A4E59E8B374C554690CE953441F>
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http://purl.uniprot.org/SHA-384/FCC10C469E8235527C728904D72323BC790D12AC15BD476BBE6F2487832F1115D2BB9A4E59E8B374C554690CE953441F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/FCC10C469E8235527C728904D72323BC790D12AC15BD476BBE6F2487832F1115D2BB9A4E59E8B374C554690CE953441F
http://www.w3.org/2000/01/rdf-schema#comment
"the T378N mutation was not found in in five patients with alternating hemiplegia of childhood"
xsd:string
http://purl.uniprot.org/uniprot/#_92F5F0EFB215E9D069CFC4CDF301426F7E2B8B2388134B088EA688B8CE157B2DC4037FBE70AE06373701A6AFD76EC856
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/FCC10C469E8235527C728904D72323BC790D12AC15BD476BBE6F2487832F1115D2BB9A4E59E8B374C554690CE953441F
http://purl.uniprot.org/uniprot/B3KW93
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FCC10C469E8235527C728904D72323BC790D12AC15BD476BBE6F2487832F1115D2BB9A4E59E8B374C554690CE953441F
http://purl.uniprot.org/uniprot/#_B3KW93-mappedCitation-18811707
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FCC10C469E8235527C728904D72323BC790D12AC15BD476BBE6F2487832F1115D2BB9A4E59E8B374C554690CE953441F