Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_assertion> ?p ?o ?g. }
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- NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_assertion type Assertion NP1159303.RAJ4ZgNHxP5HBg7qkfHFk7BMlj7R-e-AqWNYX_aeXiCis130_head.
- 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.