Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_assertion> ?p ?o ?g. }
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- NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_assertion type Assertion NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_head.
- NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_assertion description "[The t(12;21)(p13;q22) translocation is the most common chromosomal abnormality yet identified in any pediatric leukemia and gives rise to the TEL-AML1 fusion product.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_provenance.
- NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_assertion evidence source_evidence_literature NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_provenance.
- NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_assertion SIO_000772 14726384 NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_provenance.
- NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_assertion wasDerivedFrom befree-2016 NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_provenance.
- NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_assertion wasGeneratedBy ECO_0000203 NP428162.RAA1cLr4ISXsmIAw7HbLE3gF8qWKjivfy3KC4a9Ls_JJ0130_provenance.