Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.
- NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_assertion description "[When the NAT1*10 heterozygote and other genotypes without NAT1*10 allele were considered as low risk genotypes, NAT1*10/NAT1*10 had a significantly higher risk of PCa (OR = 2.4, 95% CI; 1.0-5.6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.
- NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_assertion evidence source_evidence_literature NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.
- NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_assertion SIO_000772 10211944 NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.
- NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_assertion wasDerivedFrom befree-20140225 NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.
- NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_assertion wasGeneratedBy ECO_0000203 NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP707636.RAjm-m6OeXjIyo-i9rqLHVnOtqG5Lj7CSG6md2ruJVF9s130_provenance.