Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.
- NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_assertion description "[In previous studies, genotypes conferring lower NQO1 activity have been associated with an increased risk of acute leukemia, particularly infant leukemia carrying MLL/AF4 fusion genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.
- NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_assertion evidence source_evidence_literature NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.
- NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_assertion SIO_000772 15590400 NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.
- NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_assertion wasDerivedFrom befree-2016 NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.
- NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_assertion wasGeneratedBy ECO_0000203 NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.
- befree-2016 importedOn "2016-02-19" NP472156.RA78avRV1Wc3XEzAW6v-u0wEaDzGcwQt0djUEGmuztrnI130_provenance.