Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.
- NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_assertion description "[Taken together, our data identify distinct mechanisms underlying ectopic MEF2C expression in T-ALL, either as a downstream target of NKX2-5, or via chromosomal aberrations deleting proximal gene regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.
- NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_assertion evidence source_evidence_literature NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.
- NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_assertion SIO_000772 18079734 NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.
- NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_assertion wasDerivedFrom befree-20140225 NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.
- NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_assertion wasGeneratedBy ECO_0000203 NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP872872.RAtsxVAyuodYWG-LWXlXE2mDRX4swotvxuL_B_Ep0uloc130_provenance.