Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.
- NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_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." NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.
- NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_assertion evidence source_evidence_literature NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.
- NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_assertion SIO_000772 23640996 NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.
- NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_assertion wasDerivedFrom befree-2016 NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.
- NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_assertion wasGeneratedBy ECO_0000203 NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1074748.RAED-5uHytPRL0YoQPqqDLXMJUf25GXVqVipcj88Pr_UM130_provenance.