Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_assertion> ?p ?o ?g. }
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- NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_assertion type Assertion NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_head.
- NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_assertion description "[Our finding of the ALL1 duplication as a consistent defect in patients with +11 represents the first identification of a specific gene rearrangement associated with recurrent trisomy in human cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.
- NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_assertion evidence source_evidence_literature NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.
- NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_assertion SIO_000772 8640834 NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.
- NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_assertion wasDerivedFrom befree-20140225 NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.
- NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_assertion wasGeneratedBy ECO_0000203 NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.