Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.
- NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_assertion description "[MYC rearrangement is a recurring genetic abnormality in several aggressive B-cell lymphomas including: Burkitt lymphoma, diffuse large B-cell lymphoma; B-cell lymphoma, unclassifiable with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma; rare de novo acute lymphoblastic lymphoma/leukemia, transformed follicular lymphoma, and plasmablastic lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.
- NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_assertion evidence source_evidence_literature NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.
- NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_assertion SIO_000772 21490439 NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.
- NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_assertion wasDerivedFrom befree-2016 NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.
- NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_assertion wasGeneratedBy ECO_0000203 NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.
- befree-2016 importedOn "2016-02-19" NP886917.RAcNpNVP27Efr-9htEsgkfvrRcCtJxNVzJFbBk-P9Ncl4130_provenance.