Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.
- NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_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." NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.
- NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_assertion evidence source_evidence_literature NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.
- NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_assertion SIO_000772 23603912 NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.
- NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_assertion wasDerivedFrom befree-20140225 NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.
- NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_assertion wasGeneratedBy ECO_0000203 NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP609740.RA0FQSEfIudsWizW1R2tkxBEXaaLU3cVd_zTG2qFI9oJk130_provenance.