Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.
- NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_assertion description "[The frequency of chromosomal aberrations (CA), as analysed by linear multiple regression analysis, significantly correlated with years of employment (P=0.004) and with combinations of epoxide hydrolase (EPHX) genotypes (exon 3, Tyr/His and exon 4, His/Arg), where individuals with low and medium activity EPHX genotypes exhibited higher frequencies of CA than those with high activity genotypes (P=0.044, r(2)=0.563).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.
- NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_assertion evidence source_evidence_literature NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.
- NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_assertion SIO_000772 11535253 NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.
- NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_assertion wasDerivedFrom befree-20140225 NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.
- NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_assertion wasGeneratedBy ECO_0000203 NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.
- befree-20140225 importedOn "2014-02-25" NP866310.RAxzFKeAdPwBnFcYJUdQjhFQpep85aseK3JrTP5D3ryho130_provenance.