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DESCRIBE <http://purl.uniprot.org/SHA-384/43AF1693894B3C4296B0D4D0E552439639C7E4D26195F3BB403EFAFAC12414626596C0DA3F4A5C2C401653CB393DDFBF>
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http://purl.uniprot.org/SHA-384/43AF1693894B3C4296B0D4D0E552439639C7E4D26195F3BB403EFAFAC12414626596C0DA3F4A5C2C401653CB393DDFBF
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/43AF1693894B3C4296B0D4D0E552439639C7E4D26195F3BB403EFAFAC12414626596C0DA3F4A5C2C401653CB393DDFBF
http://www.w3.org/2000/01/rdf-schema#comment
"data suggest that the CDKL3 gene is a strong candidate for nonsyndromal autosomal dominant mild mental retardation"
xsd:string
http://purl.uniprot.org/uniprot/#_026CC71CBEEFC491EBC8B22B4E1DFDF95DB403950B5B9DEFEBA6672F685D12715051A7D31370AC59BEB9294E69FFA0A4
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/43AF1693894B3C4296B0D4D0E552439639C7E4D26195F3BB403EFAFAC12414626596C0DA3F4A5C2C401653CB393DDFBF
http://purl.uniprot.org/uniprot/Q8IVW4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/43AF1693894B3C4296B0D4D0E552439639C7E4D26195F3BB403EFAFAC12414626596C0DA3F4A5C2C401653CB393DDFBF
http://purl.uniprot.org/uniprot/#_Q8IVW4-mappedCitation-18412109
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/43AF1693894B3C4296B0D4D0E552439639C7E4D26195F3BB403EFAFAC12414626596C0DA3F4A5C2C401653CB393DDFBF