Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_assertion> ?p ?o ?g. }
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- NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_assertion type Assertion NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_head.
- NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_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." NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_provenance.
- NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_assertion evidence source_evidence_literature NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_provenance.
- NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_assertion SIO_000772 8640834 NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_provenance.
- NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_assertion wasDerivedFrom befree-2016 NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_provenance.
- NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_assertion wasGeneratedBy ECO_0000203 NP1350537.RACgNe5BW33G80MMEn7aAVscNi-QMEYYKbZltGnHz1Z1I130_provenance.