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- source_evidence_literature type ECO_0000212 NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.
- NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_assertion description "[Our data suggested that the XRCC1 c.482C>T and c.1178G>A genetic polymorphisms were statistically associated with the increased risks of HCC [for c.482C>T, TT vs. CC: OR 2.05, 95% CI 1.26-3.32, P = 0.003; T vs. C: OR 1.26, 95% CI 1.04-1.51, P = 0.017; for c.1178G>A, AA vs. GG: OR 2.15, 95% CI 1.26-3.67, P = 0.004; A vs. G: OR 1.33, 95% CI 1.10-1.61, P = 0.004].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.
- NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_assertion evidence source_evidence_literature NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.
- NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_assertion SIO_000772 24570146 NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.
- NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_assertion wasDerivedFrom befree-20150227 NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.
- NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_assertion wasGeneratedBy ECO_0000203 NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP950838.RA1JHjHt6JjgNne7UVn8sPRMwfBHpY_Ie7iTIHS0ncoa4130_provenance.