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DESCRIBE <http://purl.uniprot.org/SHA-384/D2B6D69D3CBD90D779018DF274777138620DCC0B0D4498956166485DECD93031496E2731A79F1FAB66646843A843B3E2>
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http://purl.uniprot.org/SHA-384/D2B6D69D3CBD90D779018DF274777138620DCC0B0D4498956166485DECD93031496E2731A79F1FAB66646843A843B3E2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/D2B6D69D3CBD90D779018DF274777138620DCC0B0D4498956166485DECD93031496E2731A79F1FAB66646843A843B3E2
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/#_BDAAE4C0BF116CF78E6ED0E16E2E533F439CA8F2FD871F24FD08A6D07051348AEEF408A831CA3C08EE5CBEC4DE9C6B2E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/D2B6D69D3CBD90D779018DF274777138620DCC0B0D4498956166485DECD93031496E2731A79F1FAB66646843A843B3E2
http://purl.uniprot.org/uniprot/G1EPL7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D2B6D69D3CBD90D779018DF274777138620DCC0B0D4498956166485DECD93031496E2731A79F1FAB66646843A843B3E2
http://purl.uniprot.org/uniprot/#_G1EPL7-mappedCitation-25956157
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/D2B6D69D3CBD90D779018DF274777138620DCC0B0D4498956166485DECD93031496E2731A79F1FAB66646843A843B3E2