PubMed:22228096 / 90-212 JSONTXT

{"project":"c_corpus","denotations":[{"id":"T23","span":{"begin":4,"end":11},"obj":"6308"},{"id":"T24","span":{"begin":4,"end":11},"obj":"SO:0001437"},{"id":"T22","span":{"begin":4,"end":11},"obj":"CHEBI:15603"},{"id":"T25","span":{"begin":4,"end":11},"obj":"D007930"},{"id":"T26","span":{"begin":4,"end":11},"obj":"CHEBI:25017"},{"id":"T27","span":{"begin":4,"end":11},"obj":"D007930"},{"id":"T28","span":{"begin":17,"end":23},"obj":"SO:0001068"},{"id":"T29","span":{"begin":34,"end":39},"obj":"PR:Q5S006"},{"id":"T30","span":{"begin":34,"end":39},"obj":"PR:000003033"},{"id":"T31","span":{"begin":34,"end":39},"obj":"PR:Q5S007"},{"id":"T32","span":{"begin":80,"end":98},"obj":"C566739"},{"id":"T35","span":{"begin":99,"end":116},"obj":"D010300"},{"id":"T36","span":{"begin":99,"end":116},"obj":"D010300"}],"text":"The leucine-rich repeat kinase 2 (LRRK2) mutations are the most common cause of autosomal-dominant Parkinson disease (PD)."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":4,"end":32},"obj":"gene:120892"},{"id":"T1","span":{"begin":80,"end":116},"obj":"disease:C3489791"},{"id":"T2","span":{"begin":4,"end":32},"obj":"gene:120892"},{"id":"T3","span":{"begin":118,"end":120},"obj":"disease:C3489791"},{"id":"T4","span":{"begin":34,"end":39},"obj":"gene:120892"},{"id":"T5","span":{"begin":80,"end":116},"obj":"disease:C3489791"},{"id":"T6","span":{"begin":34,"end":39},"obj":"gene:120892"},{"id":"T7","span":{"begin":118,"end":120},"obj":"disease:C3489791"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"},{"id":"R3","pred":"associated_with","subj":"T4","obj":"T5"},{"id":"R4","pred":"associated_with","subj":"T6","obj":"T7"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"The leucine-rich repeat kinase 2 (LRRK2) mutations are the most common cause of autosomal-dominant Parkinson disease (PD)."}

{"project":"Allie","denotations":[{"id":"SS1_22228096_1_0","span":{"begin":4,"end":32},"obj":"expanded"},{"id":"SS2_22228096_1_0","span":{"begin":34,"end":39},"obj":"abbr"},{"id":"SS1_22228096_1_1","span":{"begin":99,"end":116},"obj":"expanded"},{"id":"SS2_22228096_1_1","span":{"begin":118,"end":120},"obj":"abbr"}],"relations":[{"id":"AE1_22228096_1_0","pred":"abbreviatedTo","subj":"SS1_22228096_1_0","obj":"SS2_22228096_1_0"},{"id":"AE1_22228096_1_1","pred":"abbreviatedTo","subj":"SS1_22228096_1_1","obj":"SS2_22228096_1_1"}],"text":"The leucine-rich repeat kinase 2 (LRRK2) mutations are the most common cause of autosomal-dominant Parkinson disease (PD)."}

{"project":"UseCases_ArguminSci_Discourse","denotations":[{"id":"T2","span":{"begin":0,"end":122},"obj":"DRI_Approach"}],"text":"The leucine-rich repeat kinase 2 (LRRK2) mutations are the most common cause of autosomal-dominant Parkinson disease (PD)."}

{"project":"PubMed_ArguminSci","denotations":[{"id":"T1","span":{"begin":0,"end":122},"obj":"DRI_Approach"}],"text":"The leucine-rich repeat kinase 2 (LRRK2) mutations are the most common cause of autosomal-dominant Parkinson disease (PD)."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":80,"end":98},"obj":"HP_0000006"},{"id":"T2","span":{"begin":99,"end":108},"obj":"HP_0001300"}],"text":"The leucine-rich repeat kinase 2 (LRRK2) mutations are the most common cause of autosomal-dominant Parkinson disease (PD)."}