Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.
- NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_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." NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.
- NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_assertion evidence source_evidence_literature NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.
- NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_assertion SIO_000772 24570146 NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.
- NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_assertion wasDerivedFrom befree-20150227 NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.
- NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_assertion wasGeneratedBy ECO_0000203 NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP972701.RAe9A6cH183urLhRvRRXGQyEMqbsfGJpB4xvgu4VhcmKc130_provenance.