Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_assertion> ?p ?o ?g. }
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- NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_assertion type Assertion NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_head.
- NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_assertion wasGeneratedBy ECO_0000203 NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_provenance.
- NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_assertion wasDerivedFrom lhgdn-20090331 NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_provenance.
- NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_assertion SIO_000772 16873670 NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_provenance.
- NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_assertion evidence source_evidence_literature NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_provenance.
- NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_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." NP146383.RACAHLCsFqTsjvMX-CJFgetT-HvpZzjLBOvlirJvVEjVA130_provenance.