Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.
- NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_assertion description "[Two non-synonymous SNPs, rs12075 (G42D) in DARC and rs2228468 (S373Y) in CCBP2, were observed to be associated with LNM in univariate analysis and remained significant after adjustment for conventional clinical risk factors, with odds ratios (ORs) of 0.54 (95% confidence interval [CI], 0.37 to 0.79) and 0.78 (95% CI, 0.62 to 0.98), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.
- NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_assertion evidence source_evidence_literature NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.
- NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_assertion SIO_000772 24260134 NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.
- NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_assertion wasDerivedFrom befree-20150227 NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.
- NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_assertion wasGeneratedBy ECO_0000203 NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP317991.RAlgkkvnxeuE211piyWvHD3-GpLJVQeYELTujnpr482Mo130_provenance.