Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.
- NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_assertion description "[EGFR mutations were detected in 21 of 71 NSCLC samples (29.6%) and in 19 of 43 adenocarcinomas (44.2%) by the RNA-based methodology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.
- NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_assertion evidence source_evidence_literature NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.
- NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_assertion SIO_000772 22117119 NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.
- NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_assertion wasDerivedFrom befree-2016 NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.
- NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_assertion wasGeneratedBy ECO_0000203 NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.
- befree-2016 importedOn "2016-02-19" NP941885.RArFO8LAQ1iIxOScNdBO70TQsgOWMA0M-oIAGa7G-tGiA130_provenance.