Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_assertion> ?p ?o ?g. }
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- NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_assertion type Assertion NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_head.
- NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_assertion description "[Here, we describe two patients bearing translocation t(11;17) presenting with a clinical diagnosis of de novo myelodysplastic syndrome (MDS): the first with sole karyotypic abnormality 46,XY,t(11;17)(p11.2; p13) and the second where it represented one of the two karyotypic abnormalities 46,XX,del(5)(q13q33)46,XX,del(5)(q13q33),t(11;17)(q24;q23).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_provenance.
- NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_assertion evidence source_evidence_literature NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_provenance.
- NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_assertion SIO_000772 23147462 NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_provenance.
- NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_assertion wasDerivedFrom befree-20140225 NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_provenance.
- NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_assertion wasGeneratedBy ECO_0000203 NP588930.RAbWSkXzHbz43g4xVhFCOsw2uQAfDqU7wmaDQW5nPVYq0130_provenance.