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DESCRIBE <http://purl.uniprot.org/SHA-384/7C893EB70048B5B9A87A0A3519F20DE8E17DB4D5072C653825D3E4C3B7096185F8450105012903B949A58F9085BF741B>
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http://purl.uniprot.org/SHA-384/7C893EB70048B5B9A87A0A3519F20DE8E17DB4D5072C653825D3E4C3B7096185F8450105012903B949A58F9085BF741B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7C893EB70048B5B9A87A0A3519F20DE8E17DB4D5072C653825D3E4C3B7096185F8450105012903B949A58F9085BF741B
http://www.w3.org/2000/01/rdf-schema#comment
"The research revealed an association between the PRKCQ rs2236379 (C>T) and Crohn's disease. The TT homozygous mutation increased the risk of developing CD and may contribute to perianal disease."
xsd:string
http://purl.uniprot.org/uniprot/#_AFDE8B7A3CC5276DC1834645CE49F20765EA5CB0810C6BEE426DDF24AC2874AAD63D963804CE473EDA8F9515FE8F0B10
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/7C893EB70048B5B9A87A0A3519F20DE8E17DB4D5072C653825D3E4C3B7096185F8450105012903B949A58F9085BF741B
http://purl.uniprot.org/uniprot/Q04759
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7C893EB70048B5B9A87A0A3519F20DE8E17DB4D5072C653825D3E4C3B7096185F8450105012903B949A58F9085BF741B
http://purl.uniprot.org/uniprot/#_Q04759-mappedCitation-30828974
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/7C893EB70048B5B9A87A0A3519F20DE8E17DB4D5072C653825D3E4C3B7096185F8450105012903B949A58F9085BF741B