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> .
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> .
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> .
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http://identifiers.org/ncbigene/
> .
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http://identifiers.org/pubmed/
> .
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http://purl.obolibrary.org/obo/eco.owl#
> .
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http://purl.org/ontology/wi/core#
> .
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> .
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> .
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http://purl.org/dc/terms/
> .
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http://www.nanopub.org/nschema#
> .
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http://rdf.disgenet.org/nanopublications.trig#
> .
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a
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lld:C0151814
a
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{
dgn-np:NP484365.RA4_VSli3kAx1b1cPALmw84JL1OiJHzfJThMyeYiS6Q8g130_assertion
dcterms:description
"[We observed that (1) pretreatment of rabbits 24 hours earlier with CCPA (100 microgram/kg IV bolus) or IB-MECA (100 or 300 microgram/kg) resulted in an approximately 35% to 40% reduction in the size of the infarct induced by 30 minutes of coronary artery occlusion and 72 hours of reperfusion compared with vehicle-treated rabbits, whereas pretreatment with the selective A(2A)AR agonist CGS 21680 (100 microgram/kg) had no effect; (2) the delayed cardioprotective effect of CCPA, but not that of IB-MECA, was completely blocked by coadministration of the highly selective A(1)AR antagonist N-0861; (3) inhibition of nitric oxide synthase (NOS) with N(omega)-nitro-L-arginine during the 30-minute occlusion abrogated the infarct-sparing action of CCPA but not that of IB-MECA; and (4) inhibition of ATP-sensitive potassium (K(ATP)) channels with sodium 5-hydroxydecanoate during the 30-minute occlusion blocked the cardioprotective effects of both CCPA and IB-MECA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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miriam-pubmed:11249876
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dgn-void:befree-20140225
pav:importedOn
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xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
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xsd:dateTime
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