Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_assertion> ?p ?o ?g. }
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- NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_assertion type Assertion NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_head.
- NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_assertion description "[A high incidence of somatically acquired point mutations in the AML1/RUNX1 gene has been reported in poorly differentiated acute myeloid leukemia (AML, M0) and in radiation-associated and therapy-related myelodysplastic syndrome (MDS) or AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_provenance.
- NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_assertion evidence source_evidence_literature NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_provenance.
- NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_assertion SIO_000772 14615365 NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_provenance.
- NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_assertion wasDerivedFrom befree-2016 NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_provenance.
- NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_assertion wasGeneratedBy ECO_0000203 NP420589.RA5RatOth34Hjfc_EcA0x9XaMLm2mNkfurNrEuf0zZy28130_provenance.