Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_assertion type Assertion NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_head.
- NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_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." NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_provenance.
- NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_assertion evidence source_evidence_literature NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_provenance.
- NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_assertion SIO_000772 8640834 NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_provenance.
- NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_assertion wasDerivedFrom befree-20140225 NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_provenance.
- NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_assertion wasGeneratedBy ECO_0000203 NP450789.RAYGlu-bDXcURDNpT_2uG_d-urTqPpcumiQk9K8_TYhxw130_provenance.