Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_assertion> ?p ?o ?g. }
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- NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_assertion type Assertion NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_head.
- NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_assertion description "[Our case confirms that the inv(11) is a rare chromosomal translocation that is associated with therapy-related or de novo myeloid malignancy and involves NUP98 and DDX10 but not MLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_provenance.
- NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_assertion evidence source_evidence_literature NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_provenance.
- NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_assertion SIO_000772 10222653 NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_provenance.
- NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_assertion wasDerivedFrom befree-2016 NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_provenance.
- NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_assertion wasGeneratedBy ECO_0000203 NP251363.RAK6C56xwSobIjxMAtGeKJN0fcwZZySULP5CQUyx6nqaY130_provenance.