Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_assertion type Assertion NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_head.
- NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_assertion wasGeneratedBy ECO_0000203 NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.
- NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_assertion wasDerivedFrom lhgdn-20090331 NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.
- NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_assertion SIO_000772 16873670 NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.
- NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_assertion evidence source_evidence_literature NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.
- NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_assertion description "[identification of a new recurrent and cryptic deletion on chromosome 11 (del (11) (p12p13)) in about 4% (6/138) of pediatric T-ALL patients that activates the LMO2 oncogene in 4 of 6 del (11) (p12p13) -positive T-ALL patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.