Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.
- NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_assertion wasGeneratedBy ECO_0000203 NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.
- NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_assertion wasDerivedFrom befree-20150227 NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.
- NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_assertion SIO_000772 12070010 NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.
- NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_assertion evidence source_evidence_literature NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.
- NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_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." NP440365.RAD-iZxw_gTkXSAlc3YRPx7VVhdmHSqYoLT3weA83HrWY130_provenance.