Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.
- NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_assertion description "[JAK2 and MPL mutations appear to exert a phenotype-modifying effect and are distinctly associated with polycythemia vera, essential thrombocythemia and primary myelofibrosis; the corresponding mutational frequencies are approximately 99, 55 and 65% for JAK2 and 0, 3 and 10% for MPL mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.
- NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_assertion evidence source_evidence_literature NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.
- NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_assertion SIO_000772 20428194 NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.
- NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_assertion wasDerivedFrom befree-2016 NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.
- NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_assertion wasGeneratedBy ECO_0000203 NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.
- befree-2016 importedOn "2016-02-19" NP809044.RAFmoknmnCSIoEymu6kDY680c7n6MH-NepZvEoG0hRF30130_provenance.