Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.
- NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_assertion description "[The JAK2 mutation was detected in 25 patients (46%); 12 of 26 patients with essential thrombocythemia (ET), 9 of 12 patients with polycyhtemia vera (PV), one of 7 patients with chronic idiopathic myelofibrosis (CIM) and one patient with unclassifiable MPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.
- NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_assertion evidence source_evidence_literature NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.
- NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_assertion SIO_000772 17249502 NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.
- NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_assertion wasDerivedFrom befree-2016 NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.
- NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_assertion wasGeneratedBy ECO_0000203 NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.
- befree-2016 importedOn "2016-02-19" NP590327.RAy6Z5K_A6oMWoDEE_xmvEVmQRMdwOuGeiikn3RtQepVo130_provenance.