Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_assertion type Assertion NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_head.
- NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_assertion description "[A recurrent chromosomal abnormality in acute myeloid leukemia is the reciprocal translocation t(8;21) that fuses RUNX1 and ETO genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_provenance.
- NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_assertion evidence source_evidence_literature NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_provenance.
- NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_assertion SIO_000772 26333776 NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_provenance.
- NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_assertion wasDerivedFrom befree-2016 NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_provenance.
- NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_assertion wasGeneratedBy ECO_0000203 NP1293589.RAFwY0-GB0tzFw7yNvow6cyevOlMR62p3ig5lnLBIzaTc130_provenance.