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- source_evidence_literature type ECO_0000212 NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.
- NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_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." NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.
- NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_assertion evidence source_evidence_literature NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.
- NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_assertion SIO_000772 9568693 NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.
- NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_assertion wasDerivedFrom befree-2016 NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.
- NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_assertion wasGeneratedBy ECO_0000203 NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1394194.RAUGXwnR1Vltfurx2mxUK5fzjBPMWXVR4aCmVAnWMVb7k130_provenance.