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- source_evidence_literature type ECO_0000212 NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.
- NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_assertion description "[The frequency of haplotype GGCT between cases and controls was significantly different in both Chinese Hui [OR (95%CI) = 4.714 (1.04-21.36)] and Han populations [OR (95%CI) = 1.723 (1.03-2.883)] (P < 0.05), implying that the haplotype GGCT of the VDR gene is associated with susceptibility to T2DM in these ethnicities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.
- NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_assertion evidence source_evidence_literature NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.
- NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_assertion SIO_000772 25501168 NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.
- NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_assertion wasDerivedFrom befree-2016 NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.
- NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_assertion wasGeneratedBy ECO_0000203 NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247492.RAoI5DgZE9pqPEXtbHEqJnpHK-N8dJLYSigIw9nuE3VAY130_provenance.