Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_assertion> ?p ?o ?g. }
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- NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_assertion type Assertion NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_head.
- NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_assertion wasGeneratedBy ECO_0000203 NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_provenance.
- NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_assertion wasDerivedFrom befree-20150227 NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_provenance.
- NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_assertion SIO_000772 24870754 NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_provenance.
- NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_assertion evidence source_evidence_literature NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_provenance.
- NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_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." NP387051.RAgc712tUMDKjJIaM0_L1PNKBOSOYO4n77Wm7rFNqzDxU130_provenance.