Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_assertion> ?p ?o ?g. }
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- NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_assertion type Assertion NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_head.
- NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_assertion description "[Although GSTT1 null genotype was insignificantly lower in ALL patients (20.9%) than controls (22.7%), it was significantly underrepresented in ANLL patients (6.5%) (P = 0.05, OR 0.24, 95% CI 0.05-1.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_provenance.
- NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_assertion evidence source_evidence_literature NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_provenance.
- NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_assertion SIO_000772 12827651 NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_provenance.
- NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_assertion wasDerivedFrom befree-2016 NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_provenance.
- NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_assertion wasGeneratedBy ECO_0000203 NP399663.RADwi0PvBLXGCywEXrc-BC8RPLs_4jO-csORH7pX2X2S4130_provenance.