Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.
- NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_assertion description "[Furthermore, by taking account of genomic mutations causing transcriptional aberrations, we could improve the sensitivity of deleterious mutation detection in known cancer driver genes (TP53, AXIN1, ARID2, RPS6KA3), and identified recurrent disruptions in putative cancer driver genes such as HNF4A, CPS1, TSC1 and THRAP3 in HCCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.
- NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_assertion evidence source_evidence_literature NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.
- NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_assertion SIO_000772 25526364 NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.
- NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_assertion wasDerivedFrom befree-2016 NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.
- NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_assertion wasGeneratedBy ECO_0000203 NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249745.RA-WmSp41RjrttHpjzugaBJSWU_MHBcuFn3Mf5n-J2t14130_provenance.