Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.
- NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_assertion description "[Significant associations were found between MTHFR C677T polymorphisms and POAG in allelic model (OR=1.39, 95% CI=1.05-1.83) and additive model (OR=1.88, 95% CI=1.04-3.43) for population-based (PB) subgroup.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.
- NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_assertion evidence source_evidence_literature NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.
- NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_assertion SIO_000772 23123730 NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.
- NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_assertion wasDerivedFrom befree-20140225 NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.
- NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_assertion wasGeneratedBy ECO_0000203 NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP156085.RABWd_v7fRBj7Bj4WYCs8sUFCvsnGFyjQ2_2oS9SYxOmk130_provenance.