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DESCRIBE <http://purl.uniprot.org/SHA-384/CA00F245214073A1EBE047C8D838203AC003F7479082D9BD2E9D0FA92AB37663517889145AF3010A4A48FEF9501B8BC2>
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http://purl.uniprot.org/SHA-384/CA00F245214073A1EBE047C8D838203AC003F7479082D9BD2E9D0FA92AB37663517889145AF3010A4A48FEF9501B8BC2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CA00F245214073A1EBE047C8D838203AC003F7479082D9BD2E9D0FA92AB37663517889145AF3010A4A48FEF9501B8BC2
http://www.w3.org/2000/01/rdf-schema#comment
"All three patients present with epilepsy and intellectual disability pinpointing the CACNA2D1 gene as an interesting candidate gene for these clinical features."
xsd:string
http://purl.uniprot.org/uniprot/#_6E78A0DCDD718C766E174EF1147863257F8AD80B365ADCA75E6A1B6443D657919EDFD4FEE1FE482C75E45B6D8DD6D97F
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CA00F245214073A1EBE047C8D838203AC003F7479082D9BD2E9D0FA92AB37663517889145AF3010A4A48FEF9501B8BC2
http://purl.uniprot.org/uniprot/B7Z658
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CA00F245214073A1EBE047C8D838203AC003F7479082D9BD2E9D0FA92AB37663517889145AF3010A4A48FEF9501B8BC2
http://purl.uniprot.org/uniprot/#_B7Z658-mappedCitation-25074461
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CA00F245214073A1EBE047C8D838203AC003F7479082D9BD2E9D0FA92AB37663517889145AF3010A4A48FEF9501B8BC2