Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.
- NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_assertion description "[In addition to mutations in genes known to be involved in leukemogenesis (ETV6, NOTCH1, JAK1, and NF1), we identified novel recurrent mutations in FAT1 (25%), FAT3 (20%), DNM2 (35%), and genes associated with epigenetic regulation (MLL2, BMI1, and DNMT3A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.
- NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_assertion evidence source_evidence_literature NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.
- NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_assertion SIO_000772 23603912 NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.
- NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_assertion wasDerivedFrom befree-20150227 NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.
- NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_assertion wasGeneratedBy ECO_0000203 NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP519049.RA_bYUDfrDDUpQTKSiTXvs4304Rip4ikEaAhLn298QhsE130_provenance.