Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.
- NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_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." NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.
- NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_assertion evidence source_evidence_literature NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.
- NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_assertion SIO_000772 21635931 NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.
- NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_assertion wasDerivedFrom befree-20150227 NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.
- NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_assertion wasGeneratedBy ECO_0000203 NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP371910.RAw9_AeHsKiH3-ZOs8HFpT0FmlcQhniHyfOi2bEwic-8I130_provenance.