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DESCRIBE <http://purl.uniprot.org/SHA-384/120842DFB73C1A1CB041ED445AD2113D92FA537886A75CF111264CCC69C438A917D5C379922B764095BD933129F38FD9>
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http://purl.uniprot.org/SHA-384/120842DFB73C1A1CB041ED445AD2113D92FA537886A75CF111264CCC69C438A917D5C379922B764095BD933129F38FD9
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/120842DFB73C1A1CB041ED445AD2113D92FA537886A75CF111264CCC69C438A917D5C379922B764095BD933129F38FD9
http://www.w3.org/2000/01/rdf-schema#comment
"Heterozygous IFNA4 variants is a cause of impaired function and CD-susceptibility genes in Chinese individuals from multiple center based study."
xsd:string
http://purl.uniprot.org/uniprot/#_D98A66357EF4A9D0FF7877DB59A17F471F875C373082C94E8EBB7F965903A49DC1ECA2C1D19B7429E681A2744E9C290E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/120842DFB73C1A1CB041ED445AD2113D92FA537886A75CF111264CCC69C438A917D5C379922B764095BD933129F38FD9
http://purl.uniprot.org/uniprot/P05014
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/120842DFB73C1A1CB041ED445AD2113D92FA537886A75CF111264CCC69C438A917D5C379922B764095BD933129F38FD9
http://purl.uniprot.org/uniprot/#_P05014-mappedCitation-26000985
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/120842DFB73C1A1CB041ED445AD2113D92FA537886A75CF111264CCC69C438A917D5C379922B764095BD933129F38FD9