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http://www.tkuhn.ch/bel2nanopub/RAAk2njFqlWNsV5AjyaJyOyCywCp7KEXaDb1I86_7k9M0#_1
http://semanticscience.org/resource/SIO_000139
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http://www.tkuhn.ch/bel2nanopub/RAAk2njFqlWNsV5AjyaJyOyCywCp7KEXaDb1I86_7k9M0#_1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://amigo.geneontology.org/amigo/term/GO:0016301
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http://purl.obolibrary.org/obo/RO_0002204
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http://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI_36080
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http://www.w3.org/1999/02/22-rdf-syntax-ns#type
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http://purl.obolibrary.org/obo/BFO_0000066
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kin(p(PFH:"PRKC Family")) -> p(HGNC:EIF6,pmod(P))
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Approximately 61,000 statements.
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Copyright (c) 2011-2012, Selventa. All rights reserved.
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BEL Framework Large Corpus Document
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1.4
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http://www.w3.org/ns/prov#value
Furthermore, eIF6 interacts in the cytoplasm with RACK1, a receptor for activated protein kinase C (PKC). RACK1 is a major component of translating ribosomes, which harbour significant amounts of PKC. Loading 60S subunits with eIF6 caused a dose-dependent translational block and impairment of 80S formation, which were reversed by expression of RACK1 and stimulation of PKC in vivo and in vitro. PKC stimulation led to eIF6 phosphorylation, and mutation of a serine residue in the carboxy terminus of eIF6 impaired RACK1/PKC-mediated translational rescue.
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http://www.w3.org/ns/prov#wasQuotedFrom
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Selventa
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2014-07-03T14:30:18.825+02:00
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