
PMC:7289100 / 4726-4961
Annnotations
LitCovid-PD-FMA-UBERON
{"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T15","span":{"begin":107,"end":122},"obj":"Body_part"},{"id":"T16","span":{"begin":187,"end":200},"obj":"Body_part"},{"id":"T17","span":{"begin":218,"end":226},"obj":"Body_part"}],"attributes":[{"id":"A15","pred":"fma_id","subj":"T15","obj":"http://purl.org/sig/ont/fma/fma62851"},{"id":"A16","pred":"fma_id","subj":"T16","obj":"http://purl.org/sig/ont/fma/fma62925"},{"id":"A17","pred":"fma_id","subj":"T17","obj":"http://purl.org/sig/ont/fma/fma62851"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
LitCovid-PD-UBERON
{"project":"LitCovid-PD-UBERON","denotations":[{"id":"T8","span":{"begin":107,"end":112},"obj":"Body_part"}],"attributes":[{"id":"A8","pred":"uberon_id","subj":"T8","obj":"http://purl.obolibrary.org/obo/UBERON_0000178"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
LitCovid-PD-MONDO
{"project":"LitCovid-PD-MONDO","denotations":[{"id":"T73","span":{"begin":25,"end":32},"obj":"Disease"},{"id":"T74","span":{"begin":34,"end":37},"obj":"Disease"},{"id":"T75","span":{"begin":45,"end":72},"obj":"Disease"},{"id":"T76","span":{"begin":56,"end":72},"obj":"Disease"}],"attributes":[{"id":"A73","pred":"mondo_id","subj":"T73","obj":"http://purl.obolibrary.org/obo/MONDO_0002610"},{"id":"A74","pred":"mondo_id","subj":"T74","obj":"http://purl.obolibrary.org/obo/MONDO_0008558"},{"id":"A75","pred":"mondo_id","subj":"T75","obj":"http://purl.obolibrary.org/obo/MONDO_0015939"},{"id":"A76","pred":"mondo_id","subj":"T76","obj":"http://purl.obolibrary.org/obo/MONDO_0015938"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
LitCovid-PD-CLO
{"project":"LitCovid-PD-CLO","denotations":[{"id":"T51","span":{"begin":107,"end":112},"obj":"http://purl.obolibrary.org/obo/UBERON_0000178"},{"id":"T52","span":{"begin":107,"end":112},"obj":"http://www.ebi.ac.uk/efo/EFO_0000296"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
LitCovid-PD-CHEBI
{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T8","span":{"begin":34,"end":37},"obj":"Chemical"},{"id":"T10","span":{"begin":187,"end":200},"obj":"Chemical"}],"attributes":[{"id":"A8","pred":"chebi_id","subj":"T8","obj":"http://purl.obolibrary.org/obo/CHEBI_16039"},{"id":"A9","pred":"chebi_id","subj":"T8","obj":"http://purl.obolibrary.org/obo/CHEBI_61402"},{"id":"A10","pred":"chebi_id","subj":"T10","obj":"http://purl.obolibrary.org/obo/CHEBI_17089"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
LitCovid-PD-HP
{"project":"LitCovid-PD-HP","denotations":[{"id":"T37","span":{"begin":25,"end":32},"obj":"Phenotype"}],"attributes":[{"id":"A37","pred":"hp_id","subj":"T37","obj":"http://purl.obolibrary.org/obo/HP_0000979"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
LitCovid-sentences
{"project":"LitCovid-sentences","denotations":[{"id":"T23","span":{"begin":0,"end":235},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
LitCovid-PMC-OGER-BB
{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T90","span":{"begin":7,"end":24},"obj":"GO:0007596"},{"id":"T91","span":{"begin":45,"end":55},"obj":"UBERON:0002405"},{"id":"T92","span":{"begin":107,"end":112},"obj":"UBERON:0000178;CL:0000233"},{"id":"T93","span":{"begin":113,"end":122},"obj":"CL:0000233"},{"id":"T94","span":{"begin":164,"end":178},"obj":"GO:0042571"},{"id":"T95","span":{"begin":187,"end":200},"obj":"CHEBI:17089;BV_11;CHEBI:17089"},{"id":"T96","span":{"begin":201,"end":210},"obj":"GO:0010467"},{"id":"T97","span":{"begin":218,"end":226},"obj":"CL:0000233"},{"id":"T98","span":{"begin":227,"end":234},"obj":"GO:0009986"},{"id":"T13859","span":{"begin":7,"end":24},"obj":"GO:0007596"},{"id":"T85079","span":{"begin":45,"end":55},"obj":"UBERON:0002405"},{"id":"T30801","span":{"begin":107,"end":112},"obj":"UBERON:0000178;CL:0000233"},{"id":"T1001","span":{"begin":113,"end":122},"obj":"CL:0000233"},{"id":"T97549","span":{"begin":164,"end":178},"obj":"GO:0042571"},{"id":"T25574","span":{"begin":187,"end":200},"obj":"CHEBI:17089;BV_11;CHEBI:17089"},{"id":"T66959","span":{"begin":201,"end":210},"obj":"GO:0010467"},{"id":"T99761","span":{"begin":218,"end":226},"obj":"CL:0000233"},{"id":"T98484","span":{"begin":227,"end":234},"obj":"GO:0009986"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
LitCovid-PubTator
{"project":"LitCovid-PubTator","denotations":[{"id":"200","span":{"begin":7,"end":32},"obj":"Disease"},{"id":"201","span":{"begin":45,"end":72},"obj":"Disease"}],"attributes":[{"id":"A200","pred":"tao:has_database_id","subj":"200","obj":"MESH:D011693"},{"id":"A201","pred":"tao:has_database_id","subj":"201","obj":"MESH:D020274"}],"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":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}
2_test
{"project":"2_test","denotations":[{"id":"32535093-17917546-4828857","span":{"begin":135,"end":136},"obj":"17917546"}],"text":"Immune thrombocytopaenic purpura (ITP) is an autoimmune systemic disease manifested by the presence of low blood platelets count (\u003c10 [5]/μl) and the production of autoantibodies against glycoproteins expressed on the platelet surface."}