Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.
- NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_assertion description "[Subsequent AMKL evolves from a pre-existing TAM clone through the acquisition of additional mutations, with major mutational targets including multiple cohesin components (53%), CTCF (20%), and EZH2, KANSL1 and other epigenetic regulators (45%), as well as common signaling pathways, such as the JAK family kinases, MPL, SH2B3 (LNK) and multiple RAS pathway genes (47%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.
- NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_assertion evidence source_evidence_literature NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.
- NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_assertion SIO_000772 24056718 NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.
- NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_assertion wasDerivedFrom befree-20140225 NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.
- NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_assertion wasGeneratedBy ECO_0000203 NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP884773.RACrnUCfU17r8wx0qksL1j3VqM_zwhTNW4p_pb2Mh0oXc130_provenance.