Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.
- NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_assertion description "[The decreased risk of metabolic syndrome observed in APOA5 -12,238C and APOA4 Ser347 carriers merely reflected the fact that the APOA5 Trp19 allele was in negative linkage disequilibrium with the common alleles of APOA5 -12,238T>C and APOA4 Thr347Ser polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.
- NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_assertion evidence source_evidence_literature NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.
- NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_assertion SIO_000772 18789138 NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.
- NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_assertion wasDerivedFrom gad-20150221 NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.
- NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_assertion wasGeneratedBy ECO_0000203 NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129915.RAlJ1lJqb1XefZg9GfxMzkm1y_sRLDuyk2cNR5v_NfdOc130_provenance.