PMC:7247521 / 24828-25288 JSONTXT

{"project":"LitCovid-PubTator","denotations":[{"id":"335","span":{"begin":140,"end":144},"obj":"Gene"},{"id":"336","span":{"begin":265,"end":269},"obj":"Disease"},{"id":"337","span":{"begin":314,"end":317},"obj":"Disease"}],"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":"The component-target-pathway-disease network. Purple polygons: PubChem ID of QFPD compounds; blue pentagrams: QFPD targets; yellow circles: KEGG pathway; red square: Therapeutic Target Database (TTD) disease term, green square: Online Mendelian Inheritance in Man (OMIN) disease term. A: MXSG, B: SGMH, C: WLS, D: XCH, E: Others. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)"}

{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T279","span":{"begin":82,"end":91},"obj":"CHEBI:36357;CHEBI:36357"},{"id":"T280","span":{"begin":260,"end":263},"obj":"NCBITaxon:9606"}],"text":"The component-target-pathway-disease network. Purple polygons: PubChem ID of QFPD compounds; blue pentagrams: QFPD targets; yellow circles: KEGG pathway; red square: Therapeutic Target Database (TTD) disease term, green square: Online Mendelian Inheritance in Man (OMIN) disease term. A: MXSG, B: SGMH, C: WLS, D: XCH, E: Others. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)"}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T164","span":{"begin":285,"end":286},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T165","span":{"begin":294,"end":295},"obj":"http://purl.obolibrary.org/obo/CLO_0001021"}],"text":"The component-target-pathway-disease network. Purple polygons: PubChem ID of QFPD compounds; blue pentagrams: QFPD targets; yellow circles: KEGG pathway; red square: Therapeutic Target Database (TTD) disease term, green square: Online Mendelian Inheritance in Man (OMIN) disease term. A: MXSG, B: SGMH, C: WLS, D: XCH, E: Others. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)"}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T144","span":{"begin":71,"end":73},"obj":"Chemical"},{"id":"T145","span":{"begin":195,"end":198},"obj":"Chemical"},{"id":"T146","span":{"begin":260,"end":263},"obj":"Chemical"}],"attributes":[{"id":"A144","pred":"chebi_id","subj":"T144","obj":"http://purl.obolibrary.org/obo/CHEBI_141439"},{"id":"A145","pred":"chebi_id","subj":"T145","obj":"http://purl.obolibrary.org/obo/CHEBI_73659"},{"id":"A146","pred":"chebi_id","subj":"T146","obj":"http://purl.obolibrary.org/obo/CHEBI_37684"}],"text":"The component-target-pathway-disease network. Purple polygons: PubChem ID of QFPD compounds; blue pentagrams: QFPD targets; yellow circles: KEGG pathway; red square: Therapeutic Target Database (TTD) disease term, green square: Online Mendelian Inheritance in Man (OMIN) disease term. A: MXSG, B: SGMH, C: WLS, D: XCH, E: Others. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)"}

{"project":"LitCovid-sentences","denotations":[{"id":"T164","span":{"begin":46,"end":62},"obj":"Sentence"},{"id":"T165","span":{"begin":63,"end":165},"obj":"Sentence"},{"id":"T166","span":{"begin":166,"end":227},"obj":"Sentence"},{"id":"T167","span":{"begin":228,"end":284},"obj":"Sentence"},{"id":"T168","span":{"begin":285,"end":321},"obj":"Sentence"},{"id":"T169","span":{"begin":322,"end":460},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"The component-target-pathway-disease network. Purple polygons: PubChem ID of QFPD compounds; blue pentagrams: QFPD targets; yellow circles: KEGG pathway; red square: Therapeutic Target Database (TTD) disease term, green square: Online Mendelian Inheritance in Man (OMIN) disease term. A: MXSG, B: SGMH, C: WLS, D: XCH, E: Others. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)"}