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DESCRIBE <http://purl.uniprot.org/SHA-384/FE8AD7CF506296809D403DDDB0EEBCEA0E400B2AE3C84C30CA40BFFE714345B99D55E3B063F0D395526B9E0E52AD5C70>
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http://purl.uniprot.org/SHA-384/FE8AD7CF506296809D403DDDB0EEBCEA0E400B2AE3C84C30CA40BFFE714345B99D55E3B063F0D395526B9E0E52AD5C70
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/FE8AD7CF506296809D403DDDB0EEBCEA0E400B2AE3C84C30CA40BFFE714345B99D55E3B063F0D395526B9E0E52AD5C70
http://www.w3.org/2000/01/rdf-schema#comment
"The p.M694del variant is associated with autosomal dominantly inherited FMF in Northern European Caucasians."
xsd:string
http://purl.uniprot.org/uniprot/#_C7D70FCFA3709BC2E2D0BADB9889E25D2B2B1CA14B1EF1C833D23440E9FBC95B8A1F7DCB57030567EBFE30F1AC5CD1FF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/FE8AD7CF506296809D403DDDB0EEBCEA0E400B2AE3C84C30CA40BFFE714345B99D55E3B063F0D395526B9E0E52AD5C70
http://purl.uniprot.org/uniprot/O15553
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FE8AD7CF506296809D403DDDB0EEBCEA0E400B2AE3C84C30CA40BFFE714345B99D55E3B063F0D395526B9E0E52AD5C70
http://purl.uniprot.org/uniprot/#_O15553-mappedCitation-27150194
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FE8AD7CF506296809D403DDDB0EEBCEA0E400B2AE3C84C30CA40BFFE714345B99D55E3B063F0D395526B9E0E52AD5C70