PubMed:15292179 / 1220-1386 JSONTXT

{"project":"sentences","denotations":[{"id":"T11","span":{"begin":16,"end":159},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"similar effect. Consistent with this finding, hyperoxia stimulated ERK-1 and ERK-2 phosphorylation, whereas DPI or N-acetyl-l-cysteine blocked such activation. Hypero"}

{"project":"2015-BEL-Sample-2","denotations":[{"id":"BEL:20000586","span":{"begin":46,"end":98},"obj":"path(MESHD:Hyperoxia) increases kin(p(MGI:Mapk1))"},{"id":"BEL:20000590","span":{"begin":46,"end":98},"obj":"path(MESHD:Hyperoxia) increases kin(p(MGI:Mapk3))"},{"id":"BEL:20000586","span":{"begin":46,"end":97},"obj":"path(MESHD:Hyperoxia) increases kin(p(MGI:Mapk1))"},{"id":"BEL:20000590","span":{"begin":46,"end":97},"obj":"path(MESHD:Hyperoxia) increases kin(p(MGI:Mapk3))"}],"text":"similar effect. Consistent with this finding, hyperoxia stimulated ERK-1 and ERK-2 phosphorylation, whereas DPI or N-acetyl-l-cysteine blocked such activation. Hypero"}