Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649978.RAMgZKEAQoKnWAFkn24t2kYmZGOO1vD8FY2CjR4pAF15Y#provenance>. }
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- source_evidence_literature type ECO_0000212 provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." provenance.
- LHGDN importedOn "2009-03-31" provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom LHGDN provenance.
- assertion SIO_000772 16873670 provenance.
- assertion evidence source_evidence_literature provenance.
- 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." provenance.