Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_assertion> ?p ?o ?g. }
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- NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_assertion type Assertion NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_head.
- NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_assertion wasGeneratedBy ECO_0000203 NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_provenance.
- NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_assertion wasDerivedFrom befree-2016 NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_provenance.
- NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_assertion SIO_000772 20980453 NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_provenance.
- NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_assertion evidence source_evidence_literature NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_provenance.
- NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_assertion description "[Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP848629.RAZBPRBIJ07XcSiG8ACh5i_bCCoCRzihW9TDHQaCzdxqk130_provenance.