Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.
- NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_assertion description "[In addition, males who carried mutant alleles of CYP2A6 had a fivefold increased risk for NPC when compared with those who carried *1A/*1A genotype (OR=5.02, 95% CI=1.82-14.14).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.
- NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_assertion evidence source_evidence_literature NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.
- NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_assertion SIO_000772 16377082 NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.
- NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_assertion wasDerivedFrom befree-20140225 NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.
- NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_assertion wasGeneratedBy ECO_0000203 NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP448869.RAQXZmp7FnjLnvNoUQ9uS298JyZ22YTPwAKvlV3_e9ZN8130_provenance.