Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.
- NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_assertion wasGeneratedBy ECO_0000203 NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.
- NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_assertion wasDerivedFrom befree-20140225 NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.
- NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_assertion SIO_000772 19899988 NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.
- NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_assertion evidence source_evidence_literature NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.
- NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_assertion description "[The G allele of the C3 IVS2 rs2250656, but not other tested C3 SNPs of rs2230205, rs10411506, rs2230199, rs339392, and rs163913, was significantly associated with a reduced risk for AMD in the Chinese population (OR 0.605, 95% CI 0.39-0.93, p = 0.023), even after adjusting for age, gender, smoking status, CFH rs1061170, CFB rs4151667, and CFB rs641153 allele status (OR 0.58, 95% CI 0.35-0.96, p = 0.033).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP382949.RACneipjC2Cb5MJLhEMSuNNrW199GjcxUIWXwNmL6r7DQ130_provenance.