Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.
- NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_assertion description "[For the first time, we associate the RFC1 80G>A and NNMT IVS -151C>T variants to an increased ALL susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.
- NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_assertion evidence source_evidence_literature NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.
- NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_assertion SIO_000772 19020309 NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.
- NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_assertion wasDerivedFrom befree-2016 NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.
- NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_assertion wasGeneratedBy ECO_0000203 NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.
- befree-2016 importedOn "2016-02-19" NP704666.RAqOn5KgPW_H9t5Vy7rmRTafPuuWj_NXMrrw-pvoXEoFo130_provenance.