Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_assertion> ?p ?o ?g. }
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- NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_assertion type Assertion NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_head.
- NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_assertion description "[It was shown that homozygotes for the GSTT1 gene deletion occur significantly more frequently in the CML patient group compared to the control group (13.17% versus 24.10% in CML patients, Chi2 = 4.40, p < 0.05; OR = 2.09; 95% CI = 1.10-3.99).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_provenance.
- NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_assertion evidence source_evidence_literature NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_provenance.
- NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_assertion SIO_000772 21254556 NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_provenance.
- NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_assertion wasDerivedFrom gad-20150221 NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_provenance.
- NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_assertion wasGeneratedBy ECO_0000203 NP104927.RAqdWvKxXsJ3jRXVA26RiFez24hPIaROzN1_Auo_XuARA130_provenance.