Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.
- NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_assertion description "[We found that genomic alterations in the Wnt signaling pathway were common among all three subtypes; however, unique combinations of pathway alterations including Wnt, VEGF and Notch drove distinct molecular and clinical phenotypes in different CRC subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.
- NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_assertion evidence source_evidence_literature NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.
- NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_assertion SIO_000772 24260186 NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.
- NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_assertion wasDerivedFrom befree-2016 NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.
- NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_assertion wasGeneratedBy ECO_0000203 NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1130137.RAphu1FvgB13RcNoJ4zNRNEwA8jZmuq0FR7N8wkMi36hs130_provenance.