Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.
- NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_assertion description "[Furthermore, in the presence of ALDH2*1/2*2, the risks for multiple intra-esophageal cancers (OR = 3.43) and for esophageal cancer with oropharyngolaryngeal and/or stomach cancer (OR = 3.95) were higher than the risks for solitary intra-esophageal cancer and for esophageal cancer alone, but these tendencies were not observed for ADH2*1/2*1 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.
- NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_assertion evidence source_evidence_literature NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.
- NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_assertion SIO_000772 11238183 NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.
- NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_assertion wasDerivedFrom befree-20140225 NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.
- NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_assertion wasGeneratedBy ECO_0000203 NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP466227.RA4tQRJbKtwFrWx8dY468v329xwG7D3W9i3KA-ihtCQtw130_provenance.