PMC:1064873 / 5601-5867 JSONTXT

Annnotations TAB JSON ListView MergeView

    LappsTest

    {"project":"LappsTest","denotations":[{"id":"T2227","span":{"begin":105,"end":109},"obj":"Protein"},{"id":"T2226","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T2225","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T2224","span":{"begin":10,"end":14},"obj":"Protein"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    2_test

    {"project":"2_test","denotations":[{"id":"15535835-8624620-4156879","span":{"begin":59,"end":61},"obj":"8624620"},{"id":"15535835-8546719-4156879","span":{"begin":59,"end":61},"obj":"8546719"},{"id":"15535835-10529123-4156879","span":{"begin":59,"end":61},"obj":"10529123"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    biosemtest

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    pmc-enju-pas

    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and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    bionlp-st-ge-2016-test-proteins

    {"project":"bionlp-st-ge-2016-test-proteins","denotations":[{"id":"T3514","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T3513","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T3512","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T3511","span":{"begin":10,"end":14},"obj":"Protein"}],"namespaces":[{"prefix":"_base","uri":"http://bionlp.dbcls.jp/ontology/ge.owl#"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    bionlp-st-ge-2016-uniprot

    {"project":"bionlp-st-ge-2016-uniprot","denotations":[{"id":"T3855","span":{"begin":33,"end":37},"obj":"http://www.uniprot.org/uniprot/P42081"},{"id":"T3853","span":{"begin":24,"end":28},"obj":"http://www.uniprot.org/uniprot/P33681"},{"id":"T3849","span":{"begin":10,"end":14},"obj":"http://www.uniprot.org/uniprot/P10747"},{"id":"T3844","span":{"begin":105,"end":108},"obj":"http://www.uniprot.org/uniprot/P01730"}],"namespaces":[{"prefix":"_base","uri":"http://www.uniprot.org/uniprot/"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    GO-BP

    {"project":"GO-BP","denotations":[{"id":"T3301","span":{"begin":179,"end":204},"obj":"http://purl.obolibrary.org/obo/GO_0042116"},{"id":"T3283","span":{"begin":251,"end":260},"obj":"http://purl.obolibrary.org/obo/GO_0023052"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    GO-CC

    {"project":"GO-CC","denotations":[{"id":"T3595","span":{"begin":238,"end":250},"obj":"http://purl.obolibrary.org/obo/GO_0009986"},{"id":"T3584","span":{"begin":238,"end":242},"obj":"http://purl.obolibrary.org/obo/GO_0005623"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    simple1

    {"project":"simple1","denotations":[{"id":"T3917","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T3916","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T3915","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T3914","span":{"begin":10,"end":14},"obj":"Protein"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    BioNLP16_DUT

    {"project":"BioNLP16_DUT","denotations":[{"id":"T6427","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T6426","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T6425","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T6424","span":{"begin":10,"end":14},"obj":"Protein"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    BioNLP16_Messiy

    {"project":"BioNLP16_Messiy","denotations":[{"id":"T4865","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T4864","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T4863","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T4862","span":{"begin":10,"end":14},"obj":"Protein"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    DLUT931

    {"project":"DLUT931","denotations":[{"id":"T5877","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T5876","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T5875","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T5874","span":{"begin":10,"end":14},"obj":"Protein"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    bionlp-st-ge-2016-test-ihmc

    {"project":"bionlp-st-ge-2016-test-ihmc","denotations":[{"id":"T6245","span":{"begin":42,"end":65},"obj":"Protein"},{"id":"T6185","span":{"begin":238,"end":250},"obj":"Entity"},{"id":"T6170","span":{"begin":10,"end":14},"obj":"Protein"},{"id":"T6214","span":{"begin":5,"end":22},"obj":"Entity"},{"id":"T6206","span":{"begin":209,"end":229},"obj":"Entity"},{"id":"T6278","span":{"begin":193,"end":204},"obj":"Entity"},{"id":"T6254","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T6314","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T6300","span":{"begin":95,"end":117},"obj":"Entity"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    bionlp-st-ge-2016-spacy-parsed

    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and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    bionlp-st-ge-2016-test-tees

    {"project":"bionlp-st-ge-2016-test-tees","denotations":[{"id":"T3789","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T3781","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T3780","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T3779","span":{"begin":10,"end":22},"obj":"Protein"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    test3

    {"project":"test3","denotations":[{"id":"T2397","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T2396","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T2395","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T2394","span":{"begin":10,"end":14},"obj":"Protein"},{"id":"T2309","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T2308","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T2307","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T2306","span":{"begin":10,"end":14},"obj":"Protein"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}

    testone

    {"project":"testone","denotations":[{"id":"T2123","span":{"begin":105,"end":108},"obj":"Protein"},{"id":"T2122","span":{"begin":33,"end":37},"obj":"Protein"},{"id":"T2121","span":{"begin":24,"end":28},"obj":"Protein"},{"id":"T2120","span":{"begin":10,"end":14},"obj":"Protein"}],"text":" and both CD28 ligands, CD80 and CD86, in the inflamed ST [18-20]. The continuing emergence of activated CD4+ T cells, even though few in number, may be crucial in sustaining the activation of macrophages and synovial fibroblasts through cell surface signaling by me"}