Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.
- NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_assertion description "[Overexpression of hMLH1 and the adenocarcinoma subtype were both independent factors that related to EGFR mutations in NSCLCs (p=0.013 and p<0.0005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.
- NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_assertion evidence source_evidence_literature NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.
- NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_assertion SIO_000772 24205245 NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.
- NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_assertion wasDerivedFrom befree-2016 NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.
- NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_assertion wasGeneratedBy ECO_0000203 NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.
- befree-2016 importedOn "2016-02-19" NP1126309.RA70wEtVcVpUcGFa7gD3xsaCDXAEsr1tC1G-XElw4-h48130_provenance.