Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_assertion> ?p ?o ?g. }
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- NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_assertion type Assertion NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_head.
- NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_assertion wasGeneratedBy ECO_0000203 NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_provenance.
- NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_assertion wasDerivedFrom befree-20150227 NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_provenance.
- NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_assertion SIO_000772 14506644 NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_provenance.
- NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_assertion evidence source_evidence_literature NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_provenance.
- NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_assertion description "[These findings suggest that an NPM/MLF1 fusion is the primary molecular abnormality in t(3;5) MDS and AML with multilineage dysplasia, and also that cases with NPM/MLF1 may be clinically distinct from other MDS-associated disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597761.RAnfwI6O4cfByFD9y2Rr0kuqkPZQOBgvi06pdJj2qGpbY130_provenance.