PubMed:8621667 / 138-237 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/8621667","sourcedb":"PubMed","sourceid":"8621667","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/8621667","text":"Common molecular variants of the angiotensinogen gene have been associated with human hypertension.","tracks":[{"project":"sentences","denotations":[{"id":"T2","span":{"begin":0,"end":99},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":99},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"T2","pred":"source","obj":"sentences"},{"subj":"T2","pred":"source","obj":"sentences"}]},{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":33,"end":48},"obj":"gene:183"},{"id":"T1","span":{"begin":86,"end":98},"obj":"disease:C0020538"}],"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":"DisGeNET5_gene_disease","denotations":[{"id":"8621667-1#33#48#gene183","span":{"begin":33,"end":48},"obj":"gene183"},{"id":"8621667-1#86#98#diseaseC0020538","span":{"begin":86,"end":98},"obj":"diseaseC0020538"}],"relations":[{"id":"33#48#gene18386#98#diseaseC0020538","pred":"associated_with","subj":"8621667-1#33#48#gene183","obj":"8621667-1#86#98#diseaseC0020538"}],"attributes":[{"subj":"8621667-1#33#48#gene183","pred":"source","obj":"DisGeNET5_gene_disease"},{"subj":"8621667-1#86#98#diseaseC0020538","pred":"source","obj":"DisGeNET5_gene_disease"}]},{"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":86,"end":98},"obj":"HP:0000822"}],"attributes":[{"subj":"AB1","pred":"source","obj":"PubCasesHPO"}]},{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":86,"end":98},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0005044"},{"subj":"T1","pred":"source","obj":"mondo_disease"}]},{"project":"HP-phenotype","denotations":[{"id":"T2","span":{"begin":86,"end":98},"obj":"Phenotype"}],"attributes":[{"id":"A2","pred":"hp_id","subj":"T2","obj":"HP:0000822"},{"subj":"T2","pred":"source","obj":"HP-phenotype"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}]},{"project":"NCBITAXON","denotations":[{"id":"T2","span":{"begin":80,"end":85},"obj":"OrganismTaxon"}],"attributes":[{"id":"A2","pred":"db_id","subj":"T2","obj":"9606"},{"subj":"T2","pred":"source","obj":"NCBITAXON"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#93e5ec","default":true},{"id":"DisGeNET","color":"#ecd993"},{"id":"DisGeNET5_gene_disease","color":"#bf93ec"},{"id":"PubCasesHPO","color":"#93eca5"},{"id":"mondo_disease","color":"#ec939a"},{"id":"HP-phenotype","color":"#93b4ec"},{"id":"NCBITAXON","color":"#ceec93"}]}]}}