PubMed:25446991 / 119-237 JSONTXT

Annnotations TAB JSON ListView MergeView

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/25446991","sourcedb":"PubMed","sourceid":"25446991","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/25446991","text":"The G2019S leucine-rich repeat kinase 2 (LRRK2) mutation is the most common cause of genetic Parkinson's disease (PD).","tracks":[{"project":"test-210614","denotations":[{"id":"25446991_6","span":{"begin":4,"end":10},"obj":"ProteinMutation"}],"attributes":[{"id":"25446991_6_ProteinMutation","pred":"proteinmutation","subj":"25446991_6","obj":"rs34637584"},{"subj":"25446991_6","pred":"source","obj":"test-210614"}]},{"project":"PubTator4TogoVar","denotations":[{"id":"25446991_6","span":{"begin":4,"end":10},"obj":"ProteinMutation"}],"attributes":[{"id":"25446991_6_ProteinMutation","pred":"proteinmutation","subj":"25446991_6","obj":"rs34637584"},{"subj":"25446991_6","pred":"source","obj":"PubTator4TogoVar"}]},{"project":"c_corpus","denotations":[{"id":"T20","span":{"begin":9,"end":18},"obj":"CHEBI:15603"},{"id":"T22","span":{"begin":11,"end":18},"obj":"6308"},{"id":"T23","span":{"begin":11,"end":18},"obj":"SO:0001437"},{"id":"T27","span":{"begin":24,"end":30},"obj":"SO:0001068"},{"id":"T28","span":{"begin":41,"end":46},"obj":"PR:Q5S006"},{"id":"T29","span":{"begin":41,"end":46},"obj":"PR:000003033"},{"id":"T30","span":{"begin":41,"end":46},"obj":"PR:Q5S007"},{"id":"T31","span":{"begin":48,"end":56},"obj":"SO:0000109"},{"id":"T36","span":{"begin":93,"end":112},"obj":"D010300"},{"id":"T37","span":{"begin":93,"end":112},"obj":"D010300"}],"attributes":[{"subj":"T20","pred":"source","obj":"c_corpus"},{"subj":"T22","pred":"source","obj":"c_corpus"},{"subj":"T23","pred":"source","obj":"c_corpus"},{"subj":"T27","pred":"source","obj":"c_corpus"},{"subj":"T28","pred":"source","obj":"c_corpus"},{"subj":"T29","pred":"source","obj":"c_corpus"},{"subj":"T30","pred":"source","obj":"c_corpus"},{"subj":"T31","pred":"source","obj":"c_corpus"},{"subj":"T36","pred":"source","obj":"c_corpus"},{"subj":"T37","pred":"source","obj":"c_corpus"}]},{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":93,"end":102},"obj":"HP_0001300"}],"attributes":[{"subj":"T1","pred":"source","obj":"PubmedHPO"}]},{"project":"PubMed_ArguminSci","denotations":[{"id":"T1","span":{"begin":0,"end":118},"obj":"DRI_Approach"}],"attributes":[{"subj":"T1","pred":"source","obj":"PubMed_ArguminSci"}]},{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":93,"end":112},"obj":"Disease"},{"id":"T2","span":{"begin":114,"end":116},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0005180"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0005180"},{"subj":"T1","pred":"source","obj":"mondo_disease"},{"subj":"T2","pred":"source","obj":"mondo_disease"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"test-210614","color":"#ec9693","default":true},{"id":"PubTator4TogoVar","color":"#93a9ec"},{"id":"c_corpus","color":"#c3ec93"},{"id":"PubmedHPO","color":"#ec93dd"},{"id":"PubMed_ArguminSci","color":"#93ece1"},{"id":"mondo_disease","color":"#ecc693"}]}]}}