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- source_evidence_literature type ECO_0000212 NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.
- NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_assertion description "[We found that AGO1 rs595961 (?(2) = 9.066, p = 0.003; odds ratio [OR] = 0.459, 95% confidence interval [CI]: 0.275-0.768) and AGO2 rs4961280 (?(2) = 4.111, p = 0.043; OR = 0.590, 95% CI: 0.353-0.986) G alleles have significantly altered the risk for AD, and also there is a significant association of GEMIN4 rs910924 (?(2) = 5.291, p = 0.021; OR = 1.913, 95% CI: 1.094-3.344) T allele with the risk for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.
- NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_assertion evidence source_evidence_literature NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.
- NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_assertion SIO_000772 25495208 NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.
- NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_assertion wasDerivedFrom befree-2016 NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.
- NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_assertion wasGeneratedBy ECO_0000203 NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246829.RAostL9WNELKdoG-fTrlrCmR4XAMsi2mU6VB5Qw6ORNt4130_provenance.