Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.
- NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_assertion description "[We observed that DICER1 rs1057035 CT/CC variant genotypes were associated with a significant decreased risk of HCC (adjusted OR = 0.79, 95% CI = 0.64-0.96) compared with wild-type TT and RAN rs3803012 AG/GG variant genotypes increased the risk of HBV persistent infection compared with AA genotype (adjusted OR = 1.35, 95% CI = 1.03-1.77).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.
- NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_assertion evidence source_evidence_literature NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.
- NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_assertion SIO_000772 23868705 NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.
- NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_assertion wasDerivedFrom befree-2016 NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.
- NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_assertion wasGeneratedBy ECO_0000203 NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1095082.RA2jcgaVELQRbKPn5NPH3tBBswEJmap5XYezl1dY51CTo130_provenance.