Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_assertion> ?p ?o ?g. }
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- NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_assertion type Assertion NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_head.
- NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_assertion description "[TEL/AML1 gene fusion that results from a cryptic t(12;21) is the most common genetic aberration in childhood B-lineage acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_provenance.
- NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_assertion evidence source_evidence_literature NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_provenance.
- NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_assertion SIO_000772 11516105 NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_provenance.
- NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_assertion wasDerivedFrom befree-2016 NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_provenance.
- NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_assertion wasGeneratedBy ECO_0000203 NP327746.RAfKQRyf1zKxPbfSgxKMFxJ7NrpmpVaHNNNbFYLQugpjM130_provenance.