Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.
- NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_assertion description "[Further analyses of DHFR, MLL, MYC, and RFC gene status in four additional human OS cell lines revealed that only gain of DHFR and MLL were associated with an inherent lower sensitivity to MTX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.
- NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_assertion evidence source_evidence_literature NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.
- NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_assertion SIO_000772 14582536 NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.
- NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_assertion wasDerivedFrom befree-20140225 NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.
- NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_assertion wasGeneratedBy ECO_0000203 NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP887195.RA4Riv_0Zgb8GJgksqpoTvw2RGT29nH37azwmwtF6SMKA130_provenance.