Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_assertion> ?p ?o ?g. }
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- NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_assertion type Assertion NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_head.
- NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_assertion wasGeneratedBy ECO_0000203 NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_provenance.
- NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_assertion wasDerivedFrom befree-2016 NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_provenance.
- NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_assertion SIO_000772 20980453 NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_provenance.
- NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_assertion evidence source_evidence_literature NP848628.RAwNVPj38HPo6AvnKam9SkM9APFxPmbE9NXxZHBkyqw3o130_provenance.
- 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.