Matches in Nanopublications for { ?s ?p "[Our results strongly support that common sequence variants of the NER pathway genes predispose susceptible individuals to increased risk of RCC and that the association may be modified by gender, history of hypertension and obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP543337.RACzJDhsYGFIvUqfYOFrkBkcd2GlhbpC9zi__dGsUurHA130_assertion description "[Our results strongly support that common sequence variants of the NER pathway genes predispose susceptible individuals to increased risk of RCC and that the association may be modified by gender, history of hypertension and obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP543337.RACzJDhsYGFIvUqfYOFrkBkcd2GlhbpC9zi__dGsUurHA130_provenance.
- NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_assertion description "[Our results strongly support that common sequence variants of the NER pathway genes predispose susceptible individuals to increased risk of RCC and that the association may be modified by gender, history of hypertension and obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_provenance.