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PBMCs were isolated by density centrifugation over Ficoll-Hypaque (density, 1.077 g/ml; Amersham Biosciences, Amersham, UK) as previously described [34]. Cells were stimulated with anti-CD3/CD28 (1 µg/ml each) for 1 h at 37°C to stimulate Th2 cytokine release in the presence or absence of FP (10−12 to 10−8M). Cytospins were prepared and GATA-3 localization determined by confocal microscopy as previously described [12]."}
GO-BP
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GO-CC
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sentences
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events-check-again
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bionlp-st-ge-2016-reference-tees
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bionlp-st-ge-2016-reference
{"project":"bionlp-st-ge-2016-reference","denotations":[{"id":"T4347","span":{"begin":521,"end":527},"obj":"Protein"},{"id":"T4348","span":{"begin":528,"end":540},"obj":"Localization"}],"relations":[{"id":"R3730","pred":"themeOf","subj":"T4347","obj":"T4348"}],"namespaces":[{"prefix":"_base","uri":"http://bionlp.dbcls.jp/ontology/ge.owl#"}],"text":"Cell Culture and PBMC Isolation\nA human T cell line (HuT-78) was purchased from ECACC European Collection of Cell Culture (Wiltshire, UK) were cultured as previously described [12]. PBMCs were isolated by density centrifugation over Ficoll-Hypaque (density, 1.077 g/ml; Amersham Biosciences, Amersham, UK) as previously described [34]. Cells were stimulated with anti-CD3/CD28 (1 µg/ml each) for 1 h at 37°C to stimulate Th2 cytokine release in the presence or absence of FP (10−12 to 10−8M). Cytospins were prepared and GATA-3 localization determined by confocal microscopy as previously described [12]."}
bionlp-st-ge-2016-uniprot
{"project":"bionlp-st-ge-2016-uniprot","denotations":[{"id":"T4464","span":{"begin":368,"end":371},"obj":"P04234"},{"id":"T4465","span":{"begin":368,"end":371},"obj":"P20963"},{"id":"T4466","span":{"begin":368,"end":371},"obj":"P09693"},{"id":"T4467","span":{"begin":368,"end":371},"obj":"P07766"},{"id":"T4468","span":{"begin":372,"end":376},"obj":"P10747"},{"id":"T4469","span":{"begin":521,"end":527},"obj":"P23771"}],"namespaces":[{"prefix":"_base","uri":"http://www.uniprot.org/uniprot/"}],"text":"Cell Culture and PBMC Isolation\nA human T cell line (HuT-78) was purchased from ECACC European Collection of Cell Culture (Wiltshire, UK) were cultured as previously described [12]. PBMCs were isolated by density centrifugation over Ficoll-Hypaque (density, 1.077 g/ml; Amersham Biosciences, Amersham, UK) as previously described [34]. Cells were stimulated with anti-CD3/CD28 (1 µg/ml each) for 1 h at 37°C to stimulate Th2 cytokine release in the presence or absence of FP (10−12 to 10−8M). Cytospins were prepared and GATA-3 localization determined by confocal microscopy as previously described [12]."}
test2
{"project":"test2","denotations":[{"id":"T4345","span":{"begin":521,"end":527},"obj":"Protein"},{"id":"T4346","span":{"begin":528,"end":540},"obj":"Localization"}],"relations":[{"id":"R3729","pred":"themeOf","subj":"T4345","obj":"T4346"}],"text":"Cell Culture and PBMC Isolation\nA human T cell line (HuT-78) was purchased from ECACC European Collection of Cell Culture (Wiltshire, UK) were cultured as previously described [12]. PBMCs were isolated by density centrifugation over Ficoll-Hypaque (density, 1.077 g/ml; Amersham Biosciences, Amersham, UK) as previously described [34]. Cells were stimulated with anti-CD3/CD28 (1 µg/ml each) for 1 h at 37°C to stimulate Th2 cytokine release in the presence or absence of FP (10−12 to 10−8M). Cytospins were prepared and GATA-3 localization determined by confocal microscopy as previously described [12]."}