Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.
- NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_assertion description "[However, up to 25% of ECs have beta-catenin nuclear accumulation without evidence of beta-catenin mutations, suggesting alterations of other molecules that can modulate the Wnt pathway, such as APC, gamma-catenin, AXIN1 and AXIN2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.
- NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_assertion evidence source_evidence_literature NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.
- NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_assertion SIO_000772 12439748 NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.
- NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_assertion wasDerivedFrom befree-20140225 NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.
- NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_assertion wasGeneratedBy ECO_0000203 NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP541893.RA0H_CU0GhplFxx6HdIdm5v3ox8jljMSVTMp7PRHrWTyo130_provenance.