Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_assertion> ?p ?o ?g. }
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- NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_assertion type Assertion NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_head.
- NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_assertion wasGeneratedBy ECO_0000203 NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.
- NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_assertion wasDerivedFrom befree-20150227 NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.
- NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_assertion SIO_000772 12850377 NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.
- NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_assertion evidence source_evidence_literature NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.
- NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_assertion description "[The cryptic translocation t(12;21)(p13;q22), which leads to the TEL-AML1 fusion gene, is the most common abnormality in childhood B-cell ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.