PubMed:17623048 / 0-134
Annnotations
PubTator4TogoVar
{"project":"PubTator4TogoVar","denotations":[{"id":"17623048_0","span":{"begin":117,"end":123},"obj":"ProteinMutation"}],"attributes":[{"id":"17623048_0_ProteinMutation","pred":"proteinmutation","subj":"17623048_0","obj":"rs33939927"}],"text":"Leucine-rich repeat kinase 2 (LRRK2)/PARK8 possesses GTPase activity that is altered in familial Parkinson's disease R1441C/G mutants."}
c_corpus
{"project":"c_corpus","denotations":[{"id":"T2","span":{"begin":0,"end":7},"obj":"6308"},{"id":"T3","span":{"begin":0,"end":7},"obj":"SO:0001437"},{"id":"T1","span":{"begin":0,"end":7},"obj":"CHEBI:15603"},{"id":"T4","span":{"begin":0,"end":7},"obj":"D007930"},{"id":"T5","span":{"begin":0,"end":7},"obj":"CHEBI:25017"},{"id":"T6","span":{"begin":0,"end":7},"obj":"D007930"},{"id":"T7","span":{"begin":13,"end":19},"obj":"SO:0001068"},{"id":"T8","span":{"begin":30,"end":35},"obj":"PR:Q5S006"},{"id":"T9","span":{"begin":30,"end":35},"obj":"PR:000003033"},{"id":"T10","span":{"begin":30,"end":35},"obj":"PR:Q5S007"},{"id":"T13","span":{"begin":37,"end":42},"obj":"PR:000003033"},{"id":"T14","span":{"begin":37,"end":42},"obj":"PR:Q5S007"},{"id":"T12","span":{"begin":37,"end":42},"obj":"607060"},{"id":"T15","span":{"begin":53,"end":59},"obj":"D020558"},{"id":"T16","span":{"begin":53,"end":68},"obj":"GO:0003924"},{"id":"T21","span":{"begin":97,"end":116},"obj":"D010300"},{"id":"T22","span":{"begin":97,"end":116},"obj":"D010300"}],"text":"Leucine-rich repeat kinase 2 (LRRK2)/PARK8 possesses GTPase activity that is altered in familial Parkinson's disease R1441C/G mutants."}
PMID_GLOBAL
{"project":"PMID_GLOBAL","denotations":[{"id":"T1","span":{"begin":8,"end":12},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":37,"end":42},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":97,"end":116},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0015404"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0011764"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0005180"}],"text":"Leucine-rich repeat kinase 2 (LRRK2)/PARK8 possesses GTPase activity that is altered in familial Parkinson's disease R1441C/G mutants."}
UseCases_ArguminSci_Discourse
{"project":"UseCases_ArguminSci_Discourse","denotations":[{"id":"T1","span":{"begin":0,"end":134},"obj":"DRI_Outcome"}],"text":"Leucine-rich repeat kinase 2 (LRRK2)/PARK8 possesses GTPase activity that is altered in familial Parkinson's disease R1441C/G mutants."}
DisGeNET5_variant_disease
{"project":"DisGeNET5_variant_disease","denotations":[{"id":"17623048-0#117#123#geners33939927","span":{"begin":117,"end":123},"obj":"geners33939927"},{"id":"17623048-0#97#116#diseaseC0030567","span":{"begin":97,"end":116},"obj":"diseaseC0030567"}],"relations":[{"id":"117#123#geners3393992797#116#diseaseC0030567","pred":"associated_with","subj":"17623048-0#117#123#geners33939927","obj":"17623048-0#97#116#diseaseC0030567"}],"text":"Leucine-rich repeat kinase 2 (LRRK2)/PARK8 possesses GTPase activity that is altered in familial Parkinson's disease R1441C/G mutants."}
DisGeNET5_gene_disease
{"project":"DisGeNET5_gene_disease","denotations":[{"id":"17623048-0#0#28#gene120892","span":{"begin":0,"end":28},"obj":"gene120892"},{"id":"17623048-0#30#35#gene120892","span":{"begin":30,"end":35},"obj":"gene120892"},{"id":"17623048-0#37#42#gene120892","span":{"begin":37,"end":42},"obj":"gene120892"},{"id":"17623048-0#97#116#diseaseC0030567","span":{"begin":97,"end":116},"obj":"diseaseC0030567"}],"relations":[{"id":"0#28#gene12089297#116#diseaseC0030567","pred":"associated_with","subj":"17623048-0#0#28#gene120892","obj":"17623048-0#97#116#diseaseC0030567"},{"id":"30#35#gene12089297#116#diseaseC0030567","pred":"associated_with","subj":"17623048-0#30#35#gene120892","obj":"17623048-0#97#116#diseaseC0030567"},{"id":"37#42#gene12089297#116#diseaseC0030567","pred":"associated_with","subj":"17623048-0#37#42#gene120892","obj":"17623048-0#97#116#diseaseC0030567"}],"text":"Leucine-rich repeat kinase 2 (LRRK2)/PARK8 possesses GTPase activity that is altered in familial Parkinson's disease R1441C/G mutants."}