Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_assertion type Assertion NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_head.
- NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_assertion description "[We show that UPD is a common chromosomal defect in myeloid malignancies, particularly in chronic myelomonocytic leukemia (CMML; 48%) and MDS/MPD-unclassifiable (38%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_provenance.
- NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_assertion evidence source_evidence_literature NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_provenance.
- NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_assertion SIO_000772 19074904 NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_provenance.
- NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_assertion wasDerivedFrom befree-20140225 NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_provenance.
- NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_assertion wasGeneratedBy ECO_0000203 NP198669.RAXX-NMUSwFqBkSEYhU9ZF4rs5uUOBOGIYUMqhIrFMCMk130_provenance.