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http://www.tkuhn.ch/bel2nanopub/RAuL6RWogkalTFoKsgL641WyzkBkslnfrp1tPBb74_IVg#_1
http://purl.obolibrary.org/obo/RO_0002204
http://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=2561
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http://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI_33697
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http://purl.obolibrary.org/obo/BFO_0000066
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http://semanticscience.org/resource/SIO_000255
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http://amigo.geneontology.org/amigo/term/GO:0001666
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http://www.w3.org/1999/02/22-rdf-syntax-ns#Statement
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TextLocation
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Review
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http://www.w3.org/2000/01/rdf-schema#label
bp(GO:"response to hypoxia") -> r(HGNC:CXCR4)
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Approximately 2000 hand curated statements drawn from 57 PubMeds.
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Copyright (c) 2011-2012, Selventa. All Rights Reserved.
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http://purl.org/dc/elements/1.1/title
BEL Framework Small Corpus Document
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Creative Commons Attribution-Non-Commercial-ShareAlike 3.0 Unported License
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1.6
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The fact that CXCR4 is a hypoxia-inducible gene provided a potential mechanistic explanation
for CXCR4 upregulation during tumour cell evolution. CXCR4- induced
cell-surface expression due to the loss of VHL function confers enhanced migratory
potential to RCC cells in response to its cognate ligand stromal-derived factor
1 (SDF1).
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http://www.w3.org/ns/prov#wasQuotedFrom
http://www.ncbi.nlm.nih.gov/pubmed/15350900
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support@belframework.org
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Selventa
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2014-07-03T14:29:30.345+02:00
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