Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.
- NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_assertion description "[Furthermore, haplotype analysis of the -1082A/G, -819T/C, and -592A/C SNPs revealed that at least five haplotypes (ATA, ACC, GCC, ACA, and ATC) were present in this Chinese population, and the -1082G/-819C/-592C (GCC) haplotype was associated with a significantly increased risk of cachexia as compared with the ATA haplotype (OR = 2.42; 95% CI 1.17, 5.00; p = 0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.
- NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_assertion evidence source_evidence_literature NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.
- NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_assertion SIO_000772 20359252 NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.
- NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_assertion wasDerivedFrom befree-20150227 NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.
- NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_assertion wasGeneratedBy ECO_0000203 NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP255007.RAXj0_vaiCNFDzWyk1LCNSOxohFJXwElUuxSS8SK7FENA130_provenance.