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- source_evidence_literature type ECO_0000212 NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.
- NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_assertion description "[Multiple logistic regression was used to calculate odds ratios (ORs) for SSNHL and M�ni�re's disease in individuals with polymorphisms in the genes: methionine synthase (MTR; rs1805087); methionine-synthase reductase (MTRR; rs1801394); nitric oxide synthase 3 (NOS3; rs1799983); caveolin 1 (Cav1; rs3840634); melatonin receptor 1B (MTNR1B; rs1387153); NAD(P)H oxidase p22(phox) subunit (NADH/NADPHp22phox; rs4673); and mitochondria 5178 (MT5178; rs28357984).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.
- NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_assertion evidence source_evidence_literature NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.
- NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_assertion SIO_000772 23560644 NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.
- NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_assertion wasDerivedFrom befree-20150227 NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.
- NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_assertion wasGeneratedBy ECO_0000203 NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP577273.RA8YBfpO42EsL4g_E-qR0_RKUxB6FKIWqJENDYpFU-yi4130_provenance.