Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_assertion> ?p ?o ?g. }
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- NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_assertion type Assertion NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_head.
- NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_assertion description "[The ALDH2 Lys and XRCC1 Gln variant alleles were associated with an increased risk of ESCC with adjusted ORs of 1.91 (95% CI, 0.96-3.80) and 1.67 (95% CI, 1.08-2.59), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_provenance.
- NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_assertion evidence source_evidence_curated NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_provenance.
- NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_assertion SIO_000772 16639733 NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_provenance.
- NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_assertion wasDerivedFrom ctd_human-20130708 NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_provenance.
- NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_assertion wasGeneratedBy ECO_0000218 NP8409.RAsw3PxcRmlRyIk4KWrTpCU2eiIlUdKxyc45c9ryGPUfg130_provenance.