Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.
- NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_assertion description "[We have shown for the first time that variants at WFS1, JAZF1, SLC30A8, CDKN2A/B, TCF7L2, KCNQ1, HMG20A, HNF4A and DUSP9 are associated with T2D in the Saudi population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.
- NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_assertion evidence source_evidence_literature NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.
- NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_assertion SIO_000772 23448427 NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.
- NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_assertion wasDerivedFrom befree-20150227 NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.
- NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_assertion wasGeneratedBy ECO_0000203 NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP841252.RAq5FNGkGSqnHb-JKjRQBM5Z83NTvK3H6G80lxf1BmAMU130_provenance.