Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_assertion> ?p ?o ?g. }
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- NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_assertion type Assertion NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_head.
- NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_assertion description "[Comparisons of gene frequencies in ALL case and control patients showed similar frequencies (54% vs 53% GSTM1 null in whites, P =.9; 40% versus 32% in blacks, P =.45; 16% versus 15% GSTT1 null in whites, P =.8; 17% versus 28% in blacks, P =.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.
- NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_assertion evidence source_evidence_literature NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.
- NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_assertion SIO_000772 12070010 NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.
- NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_assertion wasDerivedFrom gad-20150221 NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.
- NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_assertion wasGeneratedBy ECO_0000203 NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.