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- source_evidence_literature type ECO_0000212 NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.
- NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_assertion description "[A single point mutation (Val617Phe) was identified in JAK2 in 71 (97%) of 73 patients with polycythaemia vera, 29 (57%) of 51 with essential thrombocythaemia, and eight (50%) of 16 with idiopathic myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.
- NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_assertion evidence source_evidence_literature NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.
- NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_assertion SIO_000772 15781101 NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.
- NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_assertion wasDerivedFrom befree-2016 NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.
- NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_assertion wasGeneratedBy ECO_0000203 NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.
- befree-2016 importedOn "2016-02-19" NP486338.RAoGOzbDNaPgRZdH-0WN0emNTHRyvI3QSrS9-qwRxftiI130_provenance.