Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_assertion> ?p ?o ?g. }
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- NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_assertion type Assertion NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_head.
- NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_assertion description "[Mutations have also been found with lower frequency in other FAB subtype AML (6 cases), in myeloproliferative disorders (6 cases), in myelodysplastic syndrome (3 cases) and rarely in acute lymphoblastic leukemia (1 case).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_provenance.
- NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_assertion evidence source_evidence_literature NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_provenance.
- NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_assertion SIO_000772 12529654 NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_provenance.
- NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_assertion wasDerivedFrom befree-20150227 NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_provenance.
- NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_assertion wasGeneratedBy ECO_0000203 NP394503.RAXtmSJU-m5ACNW8zvXM-evBwIipT558Y-mv_OE8zCM4s130_provenance.