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http://www.nanopub.org/nschema#Nanopublication
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http://www.tkuhn.ch/bel2nanopub/RAiZSwHX6aiND7uvy_oEBmiU9g1DKp_WJeXd36VC8oWaY#_1
http://semanticscience.org/resource/SIO_000139
http://www.tkuhn.ch/bel2nanopub/RAiZSwHX6aiND7uvy_oEBmiU9g1DKp_WJeXd36VC8oWaY#_2
http://www.tkuhn.ch/bel2nanopub/RAiZSwHX6aiND7uvy_oEBmiU9g1DKp_WJeXd36VC8oWaY#_1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://amigo.geneontology.org/amigo/term/GO:0003824
http://www.tkuhn.ch/bel2nanopub/RAiZSwHX6aiND7uvy_oEBmiU9g1DKp_WJeXd36VC8oWaY#_2
http://purl.obolibrary.org/obo/RO_0002204
http://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=9071
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http://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI_36080
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http://semanticscience.org/resource/SIO_000139
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http://www.tkuhn.ch/bel2nanopub/RAiZSwHX6aiND7uvy_oEBmiU9g1DKp_WJeXd36VC8oWaY#_3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://amigo.geneontology.org/amigo/term/GO:0003824
http://www.tkuhn.ch/bel2nanopub/RAiZSwHX6aiND7uvy_oEBmiU9g1DKp_WJeXd36VC8oWaY#_4
http://purl.obolibrary.org/obo/RO_0002204
http://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=9052
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http://www.w3.org/1999/02/22-rdf-syntax-ns#type
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http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
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http://www.w3.org/2000/01/rdf-schema#label
cat(p(HGNC:PLG)) -> cat(p(HGNC:PLAU))
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http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel
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Approximately 61,000 statements.
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Copyright (c) 2011-2012, Selventa. All rights reserved.
http://resource.belframework.org/belframework/1.0/knowledge/large_corpus.bel
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BEL Framework Large Corpus Document
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1.4
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Several types of proteolytic enzymes have been identified to specifically degrade the proteins of the extracellular matrix: matrix metalloproteinases (MMPs) [5], cysteine proteases [6], and serine proteases [7]. Serine protease urokinase-type plasminogen activator (uPA) is a protease that cleaves the extracellular matrix and stimulates the conversion of plasminogen to plasmin [8]. Plasmin mediates invasion directly, by degrading matrix proteins such as collagen IV, fibronectin, and laminin, or indirectly, by activating matrix metalloproteinases MMP-2, -3, and -9 and serine protease uPA [9-12]. uPA exerts its nonproteolytic activity through its interaction with uPA receptor (uPAR), which forms the complex with integrins and controls cell adhesion and cell migration [
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http://www.ncbi.nlm.nih.gov/pubmed/15180498
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Selventa
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2014-07-03T14:30:23.984+02:00
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