Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_assertion> ?p ?o ?g. }
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- NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_assertion type Assertion NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_head.
- NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_assertion description "[Individuals who carried polymorphisms for GSTT1 null and/or high activity microsomal epoxide hydrolase (mEH 113YY+139HR or 113YY+139RR or 113YH+139RR) and/or low activity NAD(P)H:quinone oxidoreductase 1 (NQO1 187PS/SS) were 1.65, 2.49 and 13 times more likely to have MM (P(trend)=0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_provenance.
- NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_assertion evidence source_evidence_curated NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_provenance.
- NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_assertion SIO_000772 16949155 NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_provenance.
- NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_assertion wasDerivedFrom ctd_human-20150221 NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_provenance.
- NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_assertion wasGeneratedBy ECO_0000218 NP16586.RA4VXirJyoykWTDaE3ZXwVb9Rdo6kaPFOYXD3uPHAji8o130_provenance.