Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_assertion> ?p ?o ?g. }
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- NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_assertion type Assertion NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_head.
- NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_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." NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_provenance.
- NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_assertion evidence source_evidence_literature NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_provenance.
- NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_assertion SIO_000772 14615365 NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_provenance.
- NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_assertion wasDerivedFrom befree-20140225 NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_provenance.
- NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_assertion wasGeneratedBy ECO_0000203 NP592111.RATzWZZYjGZe3h-ELGCxKEgr8yVSlTCDE7sJirx6w39sI130_provenance.