Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.
- NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_assertion description "[However, no significant associations were found between XPD Lys751Gln polymorphism and EC risk when all studies pooled into the meta-analysis (Lys/Gln vs. Lys/Lys: OR 1.07, 95% CI = 0.88-1.28; Gln/Gln vs.us Lys/Lys: OR 1.25, 95% CI = 0.92-1.71; dominant model: OR 1.09, 95% CI = 0.90-1.33).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.
- NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_assertion evidence source_evidence_literature NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.
- NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_assertion SIO_000772 21667112 NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.
- NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_assertion wasDerivedFrom befree-20140225 NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.
- NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_assertion wasGeneratedBy ECO_0000203 NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP789646.RAdyaK9JILpiZETkA2SFvXwxX2pOxHm3Y1nHNWTBa44gw130_provenance.