Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.
- befree-2016 importedOn "2016-02-19" NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.
- NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_assertion wasGeneratedBy ECO_0000203 NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.
- NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_assertion wasDerivedFrom befree-2016 NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.
- NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_assertion SIO_000772 18807132 NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.
- NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_assertion evidence source_evidence_literature NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.
- NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_assertion description "[Multivariate regression analysis showed that cagE, babA2, and IL-1RN-1/2 genotypes were independent predictors of GC, but when patients with benign disorders were grouped together (NUD + DU) and compared with patients with GC, regression analysis disclosed that babA2 (P = 0.000) and IL-1B-31 gene polymorphisms (CC or CT) (P = 0.01) were the only independent markers of GC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694332.RA0mYDtyVsXBo65RlOIOxCumvvW8Gd4MzL3QZe37Tkgfc130_provenance.