Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_assertion> ?p ?o ?g. }
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- NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_assertion type Assertion NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_head.
- NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_assertion wasGeneratedBy ECO_0000203 NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_provenance.
- NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_assertion wasDerivedFrom befree-2016 NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_provenance.
- NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_assertion SIO_000772 24822274 NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_provenance.
- NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_assertion evidence source_evidence_literature NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_provenance.
- NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_assertion description "[This suggests that UGT genetic variation alters CRC risk differently by anatomical sub-site and gender and that polymorphisms in the UGT1A shared exons may have a regulatory effect on gene expression that allows for the protective effect of NSAIDs on CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1181955.RAK8G69eQ_muUHunRFOl4hAU1w6hncM6sd0ZHLlcwSzLc130_provenance.