Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.
- NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_assertion description "[A study of 222 candidate genes in type 2 diabetes reported association of variants in RAPGEF1, ENPP1, TP53, NRF1, SLC2A2, SLC2A4 and FOXC2 with type 2 diabetes in 4,805 Finnish individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.
- NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_assertion evidence source_evidence_literature NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.
- NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_assertion SIO_000772 21283750 NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.
- NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_assertion wasDerivedFrom befree-2016 NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.
- NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_assertion wasGeneratedBy ECO_0000203 NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.
- befree-2016 importedOn "2016-02-19" NP869263.RA9rDncEIq0pDkgTRI8Afuzgxy3vTvCZyPFL6IRVVwI1I130_provenance.