Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_assertion> ?p ?o ?g. }
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- NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_assertion type Assertion NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_head.
- NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_assertion description "[Our finding of the ALL1 duplication as a consistent defect in patients with +11 represents the first identification of a specific gene rearrangement associated with recurrent trisomy in human cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_provenance.
- NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_assertion evidence source_evidence_literature NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_provenance.
- NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_assertion SIO_000772 8640834 NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_provenance.
- NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_assertion wasDerivedFrom befree-20150227 NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_provenance.
- NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_assertion wasGeneratedBy ECO_0000203 NP1014195.RACRaPbbbYr0uuvmh19Olm0IXlARvnSakPTDnXKHTwV5E130_provenance.