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- source_evidence_literature type ECO_0000212 NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP284927.RAiK_eQMiuQCpFuwU0TaaW-HRQl4eaCJwHrVNhH8IglPk130_provenance.