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DESCRIBE <http://purl.uniprot.org/SHA-384/5E7DFC18F78B498E1FEBF6F42D3F7F5C5828DD871D3098ED5077CF915608317D3B4D8DCAED281464472A3A2B36B543B0>
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http://purl.uniprot.org/SHA-384/5E7DFC18F78B498E1FEBF6F42D3F7F5C5828DD871D3098ED5077CF915608317D3B4D8DCAED281464472A3A2B36B543B0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5E7DFC18F78B498E1FEBF6F42D3F7F5C5828DD871D3098ED5077CF915608317D3B4D8DCAED281464472A3A2B36B543B0
http://www.w3.org/2000/01/rdf-schema#comment
"Genetic defects are first frameshift and nonsense mutations reported in PHD2 gene and suggest that a decreased prolyl hydroxylase activity disturbing the oxygen-sensing pathway might be the cause of erythrocytosis."
xsd:string
http://purl.uniprot.org/uniprot/#_2AC7B5BE5C897696CA4AB1491ED8921C540AD8225C040EE6CD9CA30D4E257BAACA6F40B67CD6542C6DEFC0077C62A9F0
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5E7DFC18F78B498E1FEBF6F42D3F7F5C5828DD871D3098ED5077CF915608317D3B4D8DCAED281464472A3A2B36B543B0
http://purl.uniprot.org/uniprot/R4SCQ0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5E7DFC18F78B498E1FEBF6F42D3F7F5C5828DD871D3098ED5077CF915608317D3B4D8DCAED281464472A3A2B36B543B0
http://purl.uniprot.org/uniprot/#_R4SCQ0-mappedCitation-17933562
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5E7DFC18F78B498E1FEBF6F42D3F7F5C5828DD871D3098ED5077CF915608317D3B4D8DCAED281464472A3A2B36B543B0