Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.
- NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_assertion description "[These results indicated that defected E-cadherin expression might play a role in the development of malignant phenotype in NSCLC, even though the genetic mutation of E-cadherin gene is not involved in the pathogenesis of NSCLC and does not appear to be direct cause for the reduced expression of E-cadherin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.
- NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_assertion evidence source_evidence_literature NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.
- NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_assertion SIO_000772 12140137 NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.
- NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_assertion wasDerivedFrom befree-20150227 NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.
- NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_assertion wasGeneratedBy ECO_0000203 NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP299322.RAa-gwmoxY5mhqyAqw_79krgpAa9GKxbV6lTCdt23733U130_provenance.