Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_assertion type Assertion NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_head.
- NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_assertion wasGeneratedBy ECO_0000203 NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_provenance.
- NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_assertion wasDerivedFrom befree-2016 NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_provenance.
- NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_assertion SIO_000772 24870754 NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_provenance.
- NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_assertion evidence source_evidence_literature NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_provenance.
- NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_assertion description "[TEL-AML1 fusion oncogene (t 12; 21) is the most common chromosomal abnormality in childhood acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186375.RAERW88btpR4DHpiUGBMtoS6nreHWMUwmkdnAnpI71_co130_provenance.