Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.
- NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion description "[The results indicated that the genotype ratio of NQO1C(609T), RAD51(G135C) and XRCC3(C241T) in single genotype analysis showed no statistical difference between ALL patients and normal controls, which suggested that the single genotype affect onset of ALL without statistical significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.
- NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion evidence source_evidence_literature NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.
- NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion SIO_000772 19549356 NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.
- NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion wasDerivedFrom gad-20130706 NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.
- NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion wasGeneratedBy ECO_0000203 NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance.