Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.
- NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_assertion description "[Compared with recipients with the wild-type MTHFR 677CC genotype, those with the variant 677T allele showed a decreased risk of detectable acute GVHD (677CT: odds ratio, 0.8; 95% confidence interval, 0.4-1.6; 677TT: odds ratio, 0.4; 95% confidence interval, 0.2-0.8; P for trend = .01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.
- NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_assertion evidence source_evidence_literature NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.
- NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_assertion SIO_000772 16920564 NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.
- NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_assertion wasDerivedFrom befree-20140225 NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.
- NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_assertion wasGeneratedBy ECO_0000203 NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP493977.RAIyw0ky-eZURrXnDoIAURjpv-lHZvg0LMoYZiD0cnUzc130_provenance.