Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_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." NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_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.
- 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." provenance.
- 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." provenance.