PMC:7544934 / 1332-1588 JSONTXT

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    LitCovid_Glycan-Motif-Structure

    {"project":"LitCovid_Glycan-Motif-Structure","denotations":[{"id":"T1","span":{"begin":178,"end":181},"obj":"https://glytoucan.org/Structures/Glycans/G00057MO"},{"id":"T2","span":{"begin":178,"end":181},"obj":"https://glytoucan.org/Structures/Glycans/G31736BK"}],"text":"onist drug, naltrexone suppresses high fat/LPS induced pro-inflammatory cytokine release both from macrophage cells and Adipose Tissue Macrophage. Moreover, Low Dose Naltrexone (LDN) also showed its activity as an ERK1/2 inhibitor. Notably, virtual docking"}

    LitCovid-PubTator

    {"project":"LitCovid-PubTator","denotations":[{"id":"37","span":{"begin":214,"end":220},"obj":"Gene"},{"id":"45","span":{"begin":12,"end":22},"obj":"Chemical"},{"id":"46","span":{"begin":166,"end":176},"obj":"Chemical"}],"attributes":[{"id":"A37","pred":"tao:has_database_id","subj":"37","obj":"Gene:5595"},{"id":"A45","pred":"tao:has_database_id","subj":"45","obj":"MESH:D009271"},{"id":"A46","pred":"tao:has_database_id","subj":"46","obj":"MESH:D009271"}],"namespaces":[{"prefix":"Tax","uri":"https://www.ncbi.nlm.nih.gov/taxonomy/"},{"prefix":"MESH","uri":"https://id.nlm.nih.gov/mesh/"},{"prefix":"Gene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"CVCL","uri":"https://web.expasy.org/cellosaurus/CVCL_"}],"text":"onist drug, naltrexone suppresses high fat/LPS induced pro-inflammatory cytokine release both from macrophage cells and Adipose Tissue Macrophage. Moreover, Low Dose Naltrexone (LDN) also showed its activity as an ERK1/2 inhibitor. Notably, virtual docking"}

    LitCovid-sentences

    {"project":"LitCovid-sentences","denotations":[{"id":"T15","span":{"begin":147,"end":231},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"onist drug, naltrexone suppresses high fat/LPS induced pro-inflammatory cytokine release both from macrophage cells and Adipose Tissue Macrophage. Moreover, Low Dose Naltrexone (LDN) also showed its activity as an ERK1/2 inhibitor. Notably, virtual docking"}