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- source_evidence_literature type ECO_0000212 NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.
- NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_assertion description "[In particular, we focus on the role of loss-of-function mutations in TET2, gain-of-function mutations in IDH1 and IDH2, and loss-of-function mutations in ASXL1 and mutations of unclear impact in DNMT3A in AML pathogenesis and therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.
- NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_assertion evidence source_evidence_literature NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.
- NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_assertion SIO_000772 23640996 NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.
- NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_assertion wasDerivedFrom befree-20150227 NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.
- NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_assertion wasGeneratedBy ECO_0000203 NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978473.RAvAI7pC0Uvdi1GTf5IF59g3z3CLEHgwTC4M4ZWNcin8s130_provenance.