Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_assertion> ?p ?o ?g. }
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- NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_assertion type Assertion NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_head.
- NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_assertion description "[The t(16;21)(q24;q22) translocation is a rare but recurrent chromosomal abnormality associated with therapy-related myeloid malignancies and a variant of the t(8;21) translocation in which the AML1 gene on chromosome 21 is rearranged.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.
- NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_assertion evidence source_evidence_literature NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.
- NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_assertion SIO_000772 9596646 NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.
- NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_assertion wasDerivedFrom befree-20150227 NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.
- NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_assertion wasGeneratedBy ECO_0000203 NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.