Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.
- NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_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." NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.
- NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_assertion evidence source_evidence_literature NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.
- NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_assertion SIO_000772 23603912 NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.
- NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_assertion wasDerivedFrom befree-20140225 NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.
- NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_assertion wasGeneratedBy ECO_0000203 NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP638053.RA2tzXhab8GPOr7E2JFUXEVg6Ef7jgJj1BPYGCJ2Ax8v8130_provenance.