Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.
- NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_assertion description "[Similarly, there were no increased risks associated with the XRCC2 GA/AA genotype (OR, 0.98; 95% CI, 0.76-1.26 for breast cancer and OR, 0.93; 95% CI, 0.69-1.25 for ovarian cancer) or the XRCC3 CT/TT genotype (OR, 0.92; 95% CI, 0.77-1.10 for breast cancer and OR, 0.87; 95% CI, 0.71-1.08 for ovarian cancer).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.
- NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_assertion evidence source_evidence_literature NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.
- NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_assertion SIO_000772 15734952 NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.
- NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_assertion wasDerivedFrom befree-20140225 NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.
- NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_assertion wasGeneratedBy ECO_0000203 NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP238585.RAkdcmdY1s39YIg7uv7vjQakc5MnyQLMVx70z5Ti0dnTk130_provenance.