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DESCRIBE <http://purl.uniprot.org/SHA-384/75D1CB0A25E0860D46F45C0681508C74084676E7D3C6747DEDC547C6962688BB31C5C8D622205B9E281DC84FB61F122F>
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http://purl.uniprot.org/SHA-384/75D1CB0A25E0860D46F45C0681508C74084676E7D3C6747DEDC547C6962688BB31C5C8D622205B9E281DC84FB61F122F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/75D1CB0A25E0860D46F45C0681508C74084676E7D3C6747DEDC547C6962688BB31C5C8D622205B9E281DC84FB61F122F
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); Germline mutations in the CDKN1B gene encoding p27 Kip1 are a rare cause of multiple endocrine neoplasia type 1."
xsd:string
http://purl.uniprot.org/uniprot/#_51296EA670FB18630CB27F0421844703D32D6269E57CD35F2FF02CA71A22811598E365941844020D1BCF5CC2A4F5DF5A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/75D1CB0A25E0860D46F45C0681508C74084676E7D3C6747DEDC547C6962688BB31C5C8D622205B9E281DC84FB61F122F
http://purl.uniprot.org/uniprot/B4DPH2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/75D1CB0A25E0860D46F45C0681508C74084676E7D3C6747DEDC547C6962688BB31C5C8D622205B9E281DC84FB61F122F
http://purl.uniprot.org/uniprot/#_B4DPH2-mappedCitation-18673462
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/75D1CB0A25E0860D46F45C0681508C74084676E7D3C6747DEDC547C6962688BB31C5C8D622205B9E281DC84FB61F122F