Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_assertion type Assertion NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_head.
- NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_assertion description "[We report two cases of AML who presented with well-characterised cytogenetic abnormalities at presentation: t(8;21) and t(15;17) respectively, and who, after achieving complete morphological and cytogenetic remissions post-autograft, developed MDS/AML associated with monosomy 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_provenance.
- NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_assertion evidence source_evidence_literature NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_provenance.
- NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_assertion SIO_000772 9603416 NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_provenance.
- NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_assertion wasDerivedFrom befree-20150227 NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_provenance.
- NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_assertion wasGeneratedBy ECO_0000203 NP873182.RArOI5Un7Y5eKYvtTjRp5rkng3HLKeXC7sWqEV8FtLUic130_provenance.