Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP289406.RAn-AMCAWugZVGqN818-pkb9iYa0dbOK5RfM5st0eJyh4130_provenance.
- 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.