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DESCRIBE <http://purl.uniprot.org/SHA-384/C5E99D4ACF1536336BC4481387B7A60499374A0845C130B8ED365ACEF2BCBF49DC568ADE3C300AA52790259E4E66E674>
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http://purl.uniprot.org/SHA-384/C5E99D4ACF1536336BC4481387B7A60499374A0845C130B8ED365ACEF2BCBF49DC568ADE3C300AA52790259E4E66E674
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C5E99D4ACF1536336BC4481387B7A60499374A0845C130B8ED365ACEF2BCBF49DC568ADE3C300AA52790259E4E66E674
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); Mutations in the CDKN1B and AIP genes are relatively uncommon in MEN1 mutation-negative multiple endocrine neoplasia I syndrome patients."
xsd:string
http://purl.uniprot.org/uniprot/#_88D9F79A7F327C0E7CA5552E2C8DE275848FE5E43C120B89DF78AB6EEB4361EFCE43FAB4DD12B46FD949B7F77DC5088C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C5E99D4ACF1536336BC4481387B7A60499374A0845C130B8ED365ACEF2BCBF49DC568ADE3C300AA52790259E4E66E674
http://purl.uniprot.org/uniprot/A7KS94
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C5E99D4ACF1536336BC4481387B7A60499374A0845C130B8ED365ACEF2BCBF49DC568ADE3C300AA52790259E4E66E674
http://purl.uniprot.org/uniprot/#_A7KS94-mappedCitation-18710468
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C5E99D4ACF1536336BC4481387B7A60499374A0845C130B8ED365ACEF2BCBF49DC568ADE3C300AA52790259E4E66E674