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DESCRIBE <http://purl.uniprot.org/SHA-384/822D8370B9E63853B0AA1C778993A47E712BEE9A913145F1C2A037A373CB25B7E729856AFB84CFDB49AC3CB3B5B81F23>
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http://purl.uniprot.org/SHA-384/822D8370B9E63853B0AA1C778993A47E712BEE9A913145F1C2A037A373CB25B7E729856AFB84CFDB49AC3CB3B5B81F23
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/822D8370B9E63853B0AA1C778993A47E712BEE9A913145F1C2A037A373CB25B7E729856AFB84CFDB49AC3CB3B5B81F23
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/#_C6373A34BD3E14E9F1943668EABF1E56A6D8AD210AAB4226CB170AFD88CA0EF9BC7E619CB283E2CB81639B921FA9BB70
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/822D8370B9E63853B0AA1C778993A47E712BEE9A913145F1C2A037A373CB25B7E729856AFB84CFDB49AC3CB3B5B81F23
http://purl.uniprot.org/uniprot/B4DW51
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/822D8370B9E63853B0AA1C778993A47E712BEE9A913145F1C2A037A373CB25B7E729856AFB84CFDB49AC3CB3B5B81F23
http://purl.uniprot.org/uniprot/#_B4DW51-mappedCitation-25956157
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/822D8370B9E63853B0AA1C778993A47E712BEE9A913145F1C2A037A373CB25B7E729856AFB84CFDB49AC3CB3B5B81F23