Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.
- NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_assertion description "[EGFR mutations were identified in 13 (10.5%) of fully evaluated cases (11 in adenocarcinoma and two in NSCLC-NOS) including two novel mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.
- NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_assertion evidence source_evidence_literature NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.
- NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_assertion SIO_000772 21949883 NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.
- NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_assertion wasDerivedFrom befree-2016 NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.
- NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_assertion wasGeneratedBy ECO_0000203 NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.
- befree-2016 importedOn "2016-02-19" NP926670.RAsnsQtPig4Xt5eGS4lAZEvSovtQHS_QtQ_AiKIeesEfo130_provenance.