PubMed:2572590 / 190-343 JSONTXT

Annnotations TAB JSON ListView MergeView

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/2572590","sourcedb":"PubMed","sourceid":"2572590","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/2572590","text":"alpha 2-Plasmin inhibitor is the most important physiological inhibitor of fibrinolysis; hence, its deficiency results in a severe hemorrhagic diathesis.","tracks":[{"project":"sentences","denotations":[{"id":"T3","span":{"begin":0,"end":153},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":153},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"T3","pred":"source","obj":"sentences"},{"subj":"T3","pred":"source","obj":"sentences"}]},{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":0,"end":25},"obj":"gene:5345"},{"id":"T1","span":{"begin":131,"end":152},"obj":"disease:C0019087"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"attributes":[{"subj":"T0","pred":"source","obj":"DisGeNET"},{"subj":"T1","pred":"source","obj":"DisGeNET"}]},{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":131,"end":152},"obj":"HP_0001892"}],"attributes":[{"subj":"T1","pred":"source","obj":"PubmedHPO"}]},{"project":"DisGeNET5_gene_disease","denotations":[{"id":"2572590-1#0#25#gene5345","span":{"begin":0,"end":25},"obj":"gene5345"},{"id":"2572590-1#131#152#diseaseC0019087","span":{"begin":131,"end":152},"obj":"diseaseC0019087"}],"relations":[{"id":"0#25#gene5345131#152#diseaseC0019087","pred":"associated_with","subj":"2572590-1#0#25#gene5345","obj":"2572590-1#131#152#diseaseC0019087"}],"attributes":[{"subj":"2572590-1#0#25#gene5345","pred":"source","obj":"DisGeNET5_gene_disease"},{"subj":"2572590-1#131#152#diseaseC0019087","pred":"source","obj":"DisGeNET5_gene_disease"}]},{"project":"mondo_disease","denotations":[{"id":"T2","span":{"begin":131,"end":152},"obj":"Disease"}],"attributes":[{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0002243"},{"subj":"T2","pred":"source","obj":"mondo_disease"}]},{"project":"HP-phenotype","denotations":[{"id":"T1","span":{"begin":131,"end":152},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0001892"},{"subj":"T1","pred":"source","obj":"HP-phenotype"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#ec93de","default":true},{"id":"DisGeNET","color":"#93ece0"},{"id":"PubmedHPO","color":"#ecc693"},{"id":"DisGeNET5_gene_disease","color":"#ac93ec"},{"id":"mondo_disease","color":"#94ec93"},{"id":"HP-phenotype","color":"#ec93ae"}]}]}}