Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.
- NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_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." NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.
- NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_assertion evidence source_evidence_literature NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.
- NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_assertion SIO_000772 12070010 NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.
- NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_assertion wasDerivedFrom befree-20140225 NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.
- NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_assertion wasGeneratedBy ECO_0000203 NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722028.RA8ypwYyMpcR8CKWMQNczKN8L8gx1bX5eUDk-N6uL8Qtc130_provenance.