Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP528654.RAZlPnbDCf6YhPodDqUXQR9Os2dtxR_J3cpCJmylrvwvM130_provenance.