Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.
- NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_assertion description "[Results confirm high frequencies of RAS and other activated signaling mutations (10/12 AMLs) and identify new recurrent mutations in splicing factors (5/12 AMLs in SF3B1 and 2/12 AMLs in U2AF1), IKZF1 (3/12 AMLs), and TP53 (3/12 AMLs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.
- NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_assertion evidence source_evidence_literature NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.
- NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_assertion SIO_000772 25331116 NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.
- NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_assertion wasDerivedFrom befree-2016 NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.
- NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_assertion wasGeneratedBy ECO_0000203 NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.
- befree-2016 importedOn "2016-02-19" NP1230888.RADLQf8ypkZgPqqSML9nocyDPUKfCZDOrbzLR1KBK7f7E130_provenance.