Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.
- NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_assertion description "[Through sequencing or genotyping of ~150,000 individuals across 5 ancestry groups, we identified 12 rare protein-truncating variants in SLC30A8, which encodes an islet zinc transporter (ZnT8) and harbors a common variant (p.Trp325Arg) associated with T2D risk and glucose and proinsulin levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.
- NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_assertion evidence source_evidence_literature NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.
- NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_assertion SIO_000772 24584071 NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.
- NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_assertion wasDerivedFrom befree-2016 NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.
- NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_assertion wasGeneratedBy ECO_0000203 NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.
- befree-2016 importedOn "2016-02-19" NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_provenance.