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DESCRIBE <http://purl.uniprot.org/SHA-384/45D1D99C4A6C0068F530C1D3B53BC5A24AB28715A51DE80685E538899FD69850F123AE9539183065723AEC1AAD39B496>
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http://purl.uniprot.org/SHA-384/45D1D99C4A6C0068F530C1D3B53BC5A24AB28715A51DE80685E538899FD69850F123AE9539183065723AEC1AAD39B496
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/45D1D99C4A6C0068F530C1D3B53BC5A24AB28715A51DE80685E538899FD69850F123AE9539183065723AEC1AAD39B496
http://www.w3.org/2000/01/rdf-schema#comment
"The per-allele risk of Crohn disease was markedly higher for Leu1007fsinsC than for Arg702Trp and Gly908Arg variants of NOD2 gene."
xsd:string
http://purl.uniprot.org/uniprot/#_D054701C5E8AE3129C3095F44ABFBCA5A6EDC6A71C9F50E4E63C5F413AB24B7E63A87A3A64A5A3E6007900B40BC006F2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/45D1D99C4A6C0068F530C1D3B53BC5A24AB28715A51DE80685E538899FD69850F123AE9539183065723AEC1AAD39B496
http://purl.uniprot.org/uniprot/D6CHF9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/45D1D99C4A6C0068F530C1D3B53BC5A24AB28715A51DE80685E538899FD69850F123AE9539183065723AEC1AAD39B496
http://purl.uniprot.org/uniprot/#_D6CHF9-mappedCitation-19713276
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/45D1D99C4A6C0068F530C1D3B53BC5A24AB28715A51DE80685E538899FD69850F123AE9539183065723AEC1AAD39B496