Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.
- NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_assertion description "[Our findings show deficits in mTOR-dependent translation initiation in MDD particularly via the p70S6K/eIF4B pathway, and indicate a potential association between marked deficits in synaptic proteins and dysregulation of mTOR signaling in MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.
- NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_assertion evidence source_evidence_literature NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.
- NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_assertion SIO_000772 21635931 NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.
- NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_assertion wasDerivedFrom befree-2016 NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.
- NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_assertion wasGeneratedBy ECO_0000203 NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.
- befree-2016 importedOn "2016-02-19" NP898903.RAT6c6HWDdl1_0oK1P3ni9ulTgi470UKhtVno5ORbIO7A130_provenance.