Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP209522.RAUdTnYrdVx20Y-ZpI5f19jawvU50ls3ZgMJ9XUWX19Fg130_provenance.
- 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.