Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion type Assertion NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_head.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion wasGeneratedBy ECO_0000203 NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion wasDerivedFrom befree-2016 NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion SIO_000772 19808697 NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion evidence source_evidence_literature NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.
- NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_assertion description "[Somatic mutation of the AML1/RUNX1(RUNX1) gene is seen in acute myeloid leukemia (AML) M0 subtype and in AML transformed from myelodysplastic syndrome, but the impact of this gene mutation on survival in AML patients remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767723.RAVIGXpvgXYN2YLSnNsPa6doj2Cewk0tUIHf3Fl3Zve60130_provenance.