Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.
- NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_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." NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.
- NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_assertion evidence source_evidence_literature NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.
- NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_assertion SIO_000772 12070010 NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.
- NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_assertion wasDerivedFrom gad-20150221 NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.
- NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_assertion wasGeneratedBy ECO_0000203 NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.
- gad-20150221 importedOn "2015-02-21" NP74770.RA6lSVU3w8w1StQnVAIIoLAdRQhIA9qymN8ulwoXg0o4A130_provenance.