Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_assertion> ?p ?o ?g. }
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- NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_assertion type Assertion NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_head.
- NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_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." NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_provenance.
- NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_assertion evidence source_evidence_literature NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_provenance.
- NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_assertion SIO_000772 14726384 NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_provenance.
- NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_assertion wasDerivedFrom befree-20140225 NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_provenance.
- NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_assertion wasGeneratedBy ECO_0000203 NP419206.RAkVzuglY0z3uYLv-0KaN612vY-9SGqpixZ-NL4Pox3WA130_provenance.