Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.
- NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_assertion description "[These results implicate two variants at 4q21 and 12q24 and further highlight three ADH variants in UADT cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.
- NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_assertion evidence source_evidence_literature NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.
- NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_assertion SIO_000772 21437268 NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.
- NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_assertion wasDerivedFrom befree-20150227 NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.
- NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_assertion wasGeneratedBy ECO_0000203 NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP257679.RAlX7UhKGTmYYKLCnvS-GWNtjIecMzpHb7FFg0v3paRk0130_provenance.