Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.
- NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_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." NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.
- NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_assertion evidence source_evidence_literature NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.
- NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_assertion SIO_000772 21635931 NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.
- NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_assertion wasDerivedFrom befree-2016 NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.
- NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_assertion wasGeneratedBy ECO_0000203 NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.
- befree-2016 importedOn "2016-02-19" NP898897.RAaa1F05N3koUaj2GaLTh7IGPWfr-QrGnPN_7BFRbVa6o130_provenance.