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http://www.tkuhn.ch/bel2nanopub/RAdZt4RXJpXMHhRN--oQkiqZlC5SnVhGcigR9_UQ-4Gmk
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
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http://www.tkuhn.ch/bel2nanopub/RAdZt4RXJpXMHhRN--oQkiqZlC5SnVhGcigR9_UQ-4Gmk#_1
http://purl.obolibrary.org/obo/RO_0002204
http://rgd.mcw.edu/rgdweb/report/gene/main.html?id=621163
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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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p(RGD:Mif) -> p(RGD:Src,pmod(P,Y))
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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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Treatment of MIF (10 microg/ml) led to phosphorylation of multiple cellular proteins of 60, 34 and 30 kDa in comparison with the control and the phosphorylated 60 kDa protein was considered to be an autophosphorylated member of the Src tyrosine kinases and autophosphorylation was enhanced at 3 minutes after stimulation but the protein level was sustained up to 1 hour. Further, treatment of PP2, a selective inhibitor of Src kinases markedly suppressed the upregulation of MMP13 induced by MIF. Thus, MIF enhanced the kinase activity but protein level was not increased.
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http://www.w3.org/ns/prov#wasQuotedFrom
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http://www.w3.org/2000/01/rdf-schema#label
Selventa
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2014-07-03T14:29:59.897+02:00
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