Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.
- NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_assertion wasGeneratedBy ECO_0000203 NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.
- NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_assertion wasDerivedFrom befree-20150227 NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.
- NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_assertion SIO_000772 22306120 NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.
- NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_assertion evidence source_evidence_literature NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.
- NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_assertion description "[The genotype frequency of the Ser/Ser of OGG1-Ser326Cys was significantly different in the cortical and mixed-type cataract group (P = 0.014; OR, 0.591; 95% CI, 0.391-0.893; and P = 0.035; OR, 0.639; 95% CI, 0.425-0.960; respectively), and the Cys/Cys genotype of OGG1-Ser326Cys was significantly different in the mixed-type cataract group (P = 0.012; OR, 2.610; 95% CI, 1.284-5.306) compared with that of healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602360.RA1O8GJp11kl-EPXprtPKeFcfK3H01-1QlwGE7b8AUImk130_provenance.