Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.
- NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_assertion description "[The study confirmed a high prevalence of genes known to be deregulated by aberrant methylation in HCC (e.g., Ras association [RalGDS/AF-6] domain family member 1, insulin-like growth factor 2, and adenomatous polyposis coli) and other solid tumors (e.g., NOTCH3) and describes potential candidate epidrivers (e.g., septin 9 and ephrin B2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.
- NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_assertion evidence source_evidence_literature NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.
- NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_assertion SIO_000772 25645722 NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.
- NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_assertion wasDerivedFrom befree-2016 NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.
- NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_assertion wasGeneratedBy ECO_0000203 NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260449.RAQfiuOSwlquHVDggF_3IbVYpteGZPxdoyAU4elP-hLfA130_provenance.