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DESCRIBE <http://purl.uniprot.org/SHA-384/A8B2FD84A8819BAD559176851FE4190B5E4EEDE02ECA1287CA05D6620BF34E59CC12440DEA90B3A8A3F0E41284442F6B>
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http://purl.uniprot.org/SHA-384/A8B2FD84A8819BAD559176851FE4190B5E4EEDE02ECA1287CA05D6620BF34E59CC12440DEA90B3A8A3F0E41284442F6B
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/A8B2FD84A8819BAD559176851FE4190B5E4EEDE02ECA1287CA05D6620BF34E59CC12440DEA90B3A8A3F0E41284442F6B
http://www.w3.org/2000/01/rdf-schema#comment
"data reinforce recent evidences that susceptibility alleles/haplotypes are shared among multiple autoimmune disorders and support a causal role for RAC2 variants in the pathogenesis of autoimmune diseases."
xsd:string
http://purl.uniprot.org/uniprot/#_792DF97F223BFD2CBD621D5805AD9F27B56055434137A245951A95DACBB5AA3830F66DCB0851C9F0685962ABA563513D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/A8B2FD84A8819BAD559176851FE4190B5E4EEDE02ECA1287CA05D6620BF34E59CC12440DEA90B3A8A3F0E41284442F6B
http://purl.uniprot.org/uniprot/B1AH80
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A8B2FD84A8819BAD559176851FE4190B5E4EEDE02ECA1287CA05D6620BF34E59CC12440DEA90B3A8A3F0E41284442F6B
http://purl.uniprot.org/uniprot/#_B1AH80-mappedCitation-21680873
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/A8B2FD84A8819BAD559176851FE4190B5E4EEDE02ECA1287CA05D6620BF34E59CC12440DEA90B3A8A3F0E41284442F6B