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DESCRIBE <http://purl.uniprot.org/SHA-384/FD6C96FA38F660E4DCAECFD34454B8464A3FB30E25F2A537FE7BBC198B09D17EEEBA2C5F18E51B37F90DD3589A130331>
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http://purl.uniprot.org/SHA-384/FD6C96FA38F660E4DCAECFD34454B8464A3FB30E25F2A537FE7BBC198B09D17EEEBA2C5F18E51B37F90DD3589A130331
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/FD6C96FA38F660E4DCAECFD34454B8464A3FB30E25F2A537FE7BBC198B09D17EEEBA2C5F18E51B37F90DD3589A130331
http://www.w3.org/2000/01/rdf-schema#comment
"Results suggest that it is the presence of rare syntenic SEC16A and MAMDC4 deletions that increases susceptibility to axial spondyloarthritis in family members who carry the HLA-B*27 allele."
xsd:string
http://purl.uniprot.org/uniprot/#_3797F237B4770D8C28E2D27EF4E1B2F770B4907A53F4E0CF955CB3168B337ECCEE5B3510A5A71198828CAE2CECFB843F
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/FD6C96FA38F660E4DCAECFD34454B8464A3FB30E25F2A537FE7BBC198B09D17EEEBA2C5F18E51B37F90DD3589A130331
http://purl.uniprot.org/uniprot/M1FXU8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FD6C96FA38F660E4DCAECFD34454B8464A3FB30E25F2A537FE7BBC198B09D17EEEBA2C5F18E51B37F90DD3589A130331
http://purl.uniprot.org/uniprot/#_M1FXU8-mappedCitation-25956157
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/FD6C96FA38F660E4DCAECFD34454B8464A3FB30E25F2A537FE7BBC198B09D17EEEBA2C5F18E51B37F90DD3589A130331