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DESCRIBE <http://purl.uniprot.org/SHA-384/EFDB02A30726FD68CC829C2B03F1C81085A3A1CF111D584B11E2DFDCB79A31D138F2EE356404D89DD72DA1B17D5DF7ED>
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http://purl.uniprot.org/SHA-384/EFDB02A30726FD68CC829C2B03F1C81085A3A1CF111D584B11E2DFDCB79A31D138F2EE356404D89DD72DA1B17D5DF7ED
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/EFDB02A30726FD68CC829C2B03F1C81085A3A1CF111D584B11E2DFDCB79A31D138F2EE356404D89DD72DA1B17D5DF7ED
http://www.w3.org/2000/01/rdf-schema#comment
"No novel variations were found in exons encoding for CDKN1B. So the mutations in CDKN1B are not common with premature ovarian failure in Han Chinese women; Observational study of gene-disease association. (HuGE Navigator)"
xsd:string
http://purl.uniprot.org/uniprot/#_AEB54BA41C3CF08202273F0AE73F6B6A74A78D31BE7677EFEABEAB23A1C042FD7EAC0EE875B3D4269CDC8DC7CBED5091
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/EFDB02A30726FD68CC829C2B03F1C81085A3A1CF111D584B11E2DFDCB79A31D138F2EE356404D89DD72DA1B17D5DF7ED
http://purl.uniprot.org/uniprot/Q9UH60
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EFDB02A30726FD68CC829C2B03F1C81085A3A1CF111D584B11E2DFDCB79A31D138F2EE356404D89DD72DA1B17D5DF7ED
http://purl.uniprot.org/uniprot/#_Q9UH60-mappedCitation-20615757
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/EFDB02A30726FD68CC829C2B03F1C81085A3A1CF111D584B11E2DFDCB79A31D138F2EE356404D89DD72DA1B17D5DF7ED