Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.
- NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_assertion description "[The frequency of either the AA genotype or A allele of RAD50_rs17166050 were significantly different in controls compared to leukemia group (ALL+AML) (p<0.0019 and p<0.0019, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.
- NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_assertion evidence source_evidence_literature NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.
- NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_assertion SIO_000772 24093751 NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.
- NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_assertion wasDerivedFrom befree-2016 NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.
- NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_assertion wasGeneratedBy ECO_0000203 NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1116167.RA75d8-F9UgXoK28_dTUSqN2BRJXxrsseWA-FngXIXVJo130_provenance.