Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_assertion> ?p ?o ?g. }
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- NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_assertion type Assertion NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_head.
- 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.
- NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_assertion evidence source_evidence_literature NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_provenance.
- NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_assertion SIO_000772 18711149 NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_provenance.
- NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_assertion wasDerivedFrom befree-20140225 NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_provenance.
- NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_assertion wasGeneratedBy ECO_0000203 NP184792.RArobb7ukmqqmrliljfN3zznTlhd1pbgDcLUNQJXcsNZs130_provenance.