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DESCRIBE <http://purl.uniprot.org/SHA-384/C7E8D12FA6E81FE81A3238B88706D1A244F7F47FC3BF721866F01D3C4CD6088BA867F2428E0E2A3F32D785A5EB89BB1D>
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http://purl.uniprot.org/SHA-384/C7E8D12FA6E81FE81A3238B88706D1A244F7F47FC3BF721866F01D3C4CD6088BA867F2428E0E2A3F32D785A5EB89BB1D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C7E8D12FA6E81FE81A3238B88706D1A244F7F47FC3BF721866F01D3C4CD6088BA867F2428E0E2A3F32D785A5EB89BB1D
http://www.w3.org/2000/01/rdf-schema#comment
"Our data strongly strengthen the hypothesis that MYT1L is the causal gene for the observed syndromal intellectual disability."
xsd:string
http://purl.uniprot.org/uniprot/#_13E639E4EFCFA146C553ECE0C847CAE6345DBFF9F096EFC53E122E19BA8507A8A1051D97F925595964EFDD5A692B0D37
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C7E8D12FA6E81FE81A3238B88706D1A244F7F47FC3BF721866F01D3C4CD6088BA867F2428E0E2A3F32D785A5EB89BB1D
http://purl.uniprot.org/uniprot/A0A3B3IS14
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C7E8D12FA6E81FE81A3238B88706D1A244F7F47FC3BF721866F01D3C4CD6088BA867F2428E0E2A3F32D785A5EB89BB1D
http://purl.uniprot.org/uniprot/#_A0A3B3IS14-mappedCitation-25232846
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C7E8D12FA6E81FE81A3238B88706D1A244F7F47FC3BF721866F01D3C4CD6088BA867F2428E0E2A3F32D785A5EB89BB1D