Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.
- NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_assertion description "[AGT T174M, GNB3 825C>T, and APOC3 -455T>C genotypes were significantly associated with MetS (P = 0.018, 0.0056, and 0.029, respectively) for female adults, whereas FABP2 A54T genotype was associated with MetS (P = 0.040) for female adolescents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.
- NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_assertion evidence source_evidence_literature NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.
- NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_assertion SIO_000772 15869758 NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.
- NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_assertion wasDerivedFrom gad-20150221 NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.
- NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_assertion wasGeneratedBy ECO_0000203 NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP52611.RAxd98eHnxmeE3d3cLIjc_irzRce8njJNaikKeBiEA2bo130_provenance.