Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.
- NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_assertion description "[The two missense variants (Asp673Asn and Ser1369Ala) and two sequence variants (ACC-->ACT, Thr759Thr and a c-->t intron variant in position -3 of the exon 16 splice acceptor site) were examined for association with NIDDM and for a possible influence on insulin and C-peptide secretion after intravenous glucose and tolbutamide loads in a random sample of unrelated, healthy, young Danish Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.
- NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_assertion evidence source_evidence_literature NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.
- NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_assertion SIO_000772 9568693 NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.
- NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_assertion wasDerivedFrom befree-20140225 NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.
- NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_assertion wasGeneratedBy ECO_0000203 NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP790809.RAx-9YeRvFnK1ApbVnPcz_BPuBEhupaN4vQcT0Hs46nNo130_provenance.