Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.
- NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_assertion description "[The corresponding lesion in Atm-deficient mouse T-ALLs is a chromosome t(12;14) translocation with Tcr? genes fused to sequences on chromosome 12; although these translocations do not activate Tcl1, they delete the Bcl11b haploinsufficient tumor suppressor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.
- NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_assertion evidence source_evidence_literature NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.
- NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_assertion SIO_000772 25486566 NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.
- NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_assertion wasDerivedFrom befree-2016 NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.
- NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_assertion wasGeneratedBy ECO_0000203 NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246089.RAPgKfICZe-9XwBpFY4YZ54yZBluHLhQ5tC4LJk4eOwmQ130_provenance.