Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP139307.RAErgf0Q1cfbyc9YlEMK-Rc1Gymg6UO7NIe_lzM4DP5bc130_provenance.