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- source_evidence_literature type ECO_0000212 NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.
- NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_assertion description "[Variant alleles of XRCC1 Arg(194)Trp (rs1799782) and ERCC4 Arg(415)Gln (rs1800067) were significantly associated with BBD [HR, 1.36; 95% confidence interval (95% CI), 1.06-1.74 and HR, 1.39; 95% CI, 1.09-1.76, respectively].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.
- NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_assertion evidence source_evidence_literature NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.
- NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_assertion SIO_000772 19124519 NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.
- NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_assertion wasDerivedFrom befree-20150227 NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.
- NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_assertion wasGeneratedBy ECO_0000203 NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779745.RALoBSVyOnF8aFO9ryvvwcK-HkdOBifNJTR9WjDGGhs0Q130_provenance.