Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.
- NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_assertion description "[The EGFR mutation is rare in SCLC patients, and EGFR mutation might occur more often in combined SCLCs than conventional patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.
- NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_assertion evidence source_evidence_literature NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.
- NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_assertion SIO_000772 22103903 NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.
- NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_assertion wasDerivedFrom befree-20150227 NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.
- NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_assertion wasGeneratedBy ECO_0000203 NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP369155.RAcRL6Sese_L6J2ezeAH535QLI4WzCIRIQXoZPWXa-B0A130_provenance.