Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.
- NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_assertion description "[In AD cases, a SNP within the same haplotype was associated with reduced RNASEN mRNA expression (P=0.013) and with miR expression changes (global P=0.007) of miRs known to be associated with cancer (e.g., let-7 family, miR-21, miR-25, miR-126 and miR15a).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.
- NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_assertion evidence source_evidence_literature NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.
- NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_assertion SIO_000772 21102586 NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.
- NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_assertion wasDerivedFrom befree-20150227 NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.
- NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_assertion wasGeneratedBy ECO_0000203 NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP995569.RATKgT8ydMX0NzUlls4YuCqxhW_pbEKlfOugTxVtMSV-k130_provenance.