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PubMed:31778855 JSONTXT

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sonoma

Id	Subject	Object	Predicate	Lexical cue
T-0	10-33	DISEASE	denotes	Birt-Hogg-Dubé syndrome
T-1	86-93	VAR	denotes	mutated
T-2	105-115	REG	denotes	pathogenic
T-3	117-140	DISEASE	denotes	Birt-Hogg-Dubé syndrome
T-4	142-146	DISEASE	denotes	BHDS
T-5	196-198	REG	denotes	by
T-6	210-218	VAR	denotes	mutation
T-7	226-236	GENE	denotes	folliculin
T-8	238-242	GENE	denotes	FLCN
T-9	297-303	VAR	denotes	mutant
T-10	304-314	GENE	denotes	folliculin
T-11	353-357	GENE	denotes	FLCN
T-12	358-367	VAR	denotes	mutations
T-13	372-378	POSREG	denotes	retain
T-14	387-400	MPA	denotes	functionality
T-15	405-415	REG	denotes	contribute
T-16	607-627	DISEASE	denotes	renal cell carcinoma
T-17	670-687	CPA	denotes	fibrofolliculomas
T-18	693-708	CPA	denotes	pulmonary cysts
T-19	836-844	VAR	denotes	deletion
T-20	887-891	GENE	denotes	FLCN
T-21	931-934	VAR	denotes	hit
T-22	962-966	GENE	denotes	FLCN
T-23	1018-1023	REG	denotes	cause
T-24	1037-1041	NEGREG	denotes	lack
T-25	1045-1055	GENE	denotes	folliculin
T-26	1224-1233	NEGREG	denotes	decreased
T-27	1234-1238	GENE	denotes	FLCN
T-28	1239-1249	MPA	denotes	expression
T-29	1275-1282	VAR	denotes	mutated
T-30	1283-1293	GENE	denotes	folliculin
T-31	1322-1332	REG	denotes	developing
T-32	1360-1364	DISEASE	denotes	BHDS
T-33	1366-1383	CPA	denotes	fibrofolliculomas
T-34	1385-1395	CPA	denotes	lung cysts
T-35	1401-1414	CPA	denotes	tumorigenesis
T-36	1455-1467	CPA	denotes	pathogenesis
T-37	1471-1475	DISEASE	denotes	BHDS
T-38	1484-1488	REG	denotes	role
T-39	1492-1496	GENE	denotes	FLCN
R-30	T-26	T-31	CauseOf	decreased,developing
R-31	T-33	T-31	ThemeOf	fibrofolliculomas,developing
R-32	T-34	T-31	ThemeOf	lung cysts,developing
R-33	T-35	T-31	ThemeOf	tumorigenesis,developing
R-34	T-37	T-36	ThemeOf	BHDS,pathogenesis
R-35	T-39	T-38	ThemeOf	FLCN,role
R-36	T-38	T-36	CauseOf	role,pathogenesis
R-0	T-1	T-2	CauseOf	mutated,pathogenic
R-1	T-9	T-13	CauseOf	mutant,retain
R-2	T-9	T-15	CauseOf	mutant,contribute
R-3	T-11	T-12	ThemeOf	FLCN,mutations
R-4	T-12	T-5	CauseOf	mutations,by
R-5	T-12	T-13	CauseOf	mutations,retain
R-6	T-12	T-15	CauseOf	mutations,contribute
R-7	T-3	T-5	ThemeOf	Birt-Hogg-Dubé syndrome,by
R-8	T-14	T-13	ThemeOf	functionality,retain
R-9	T-19	T-23	CauseOf	deletion,cause
R-10	T-19	T-24	CauseOf	deletion,lack
R-11	T-20	T-19	ThemeOf	FLCN,deletion
R-12	T-20	T-21	ThemeOf	FLCN,hit
R-13	T-4	T-5	ThemeOf	BHDS,by
R-14	T-21	T-23	CauseOf	hit,cause
R-15	T-21	T-24	CauseOf	hit,lack
R-16	T-22	T-21	ThemeOf	FLCN,hit
R-17	T-23	T-24	CauseOf	cause,lack
R-18	T-27	T-28	ThemeOf	FLCN,expression
R-19	T-28	T-26	ThemeOf	expression,decreased
R-20	T-6	T-5	CauseOf	mutation,by
R-21	T-6	T-13	CauseOf	mutation,retain
R-22	T-6	T-15	CauseOf	mutation,contribute
R-23	T-7	T-6	ThemeOf	folliculin,mutation
R-24	T-8	T-6	ThemeOf	FLCN,mutation
R-25	T-10	T-9	ThemeOf	folliculin,mutant
R-26	T-25	T-24	ThemeOf	folliculin,lack
R-27	T-30	T-29	ThemeOf	folliculin,mutated
R-28	T-32	T-31	ThemeOf	BHDS,developing
R-29	T-29	T-31	CauseOf	mutated,developing

sonoma2

Id	Subject	Object	Predicate	Lexical cue
T0	10-33	DISEASE	denotes	Birt-Hogg-Dubé syndrome
T1	43-50	NEGREG	denotes	reduced
T2	67-77	GENE	denotes	folliculin
T3	67-77	GENE	denotes	folliculin
T4	86-93	VAR	denotes	mutated
T5	94-101	GENE	denotes	protein
T6	105-115	REG	denotes	pathogenic
T7	117-140	DISEASE	denotes	Birt-Hogg-Dubé syndrome
T8	142-146	DISEASE	denotes	BHDS
T9	154-188	DISEASE	denotes	autosomal dominant cancer syndrome
T10	189-195	REG	denotes	caused
T11	210-218	VAR	denotes	mutation
T12	226-236	GENE	denotes	folliculin
T13	238-242	GENE	denotes	FLCN
T14	297-303	VAR	denotes	mutant
T15	304-323	GENE	denotes	folliculin proteins
T16	304-314	GENE	denotes	folliculin
T17	353-357	GENE	denotes	FLCN
T18	358-367	VAR	denotes	mutations
T19	387-400	MPA	denotes	functionality
T20	405-415	REG	denotes	contribute
T21	481-497	DISEASE	denotes	left renal tumor
T22	595-627	DISEASE	denotes	chromophobe renal cell carcinoma
T23	670-687	DISEASE	denotes	fibrofolliculomas
T24	693-708	DISEASE	denotes	pulmonary cysts
T25	836-844	VAR	denotes	deletion
T26	887-891	GENE	denotes	FLCN
T27	931-934	VAR	denotes	hit
T28	962-966	GENE	denotes	FLCN
T29	974-989	DISEASE	denotes	renal carcinoma
T30	1018-1023	REG	denotes	cause
T31	1037-1041	NEGREG	denotes	lack
T32	1045-1063	GENE	denotes	folliculin protein
T33	1045-1055	GENE	denotes	folliculin
T34	1102-1117	GENE	denotes	anti-folliculin
T35	1157-1184	DISEASE	denotes	chromophobe renal carcinoma
T36	1224-1233	NEGREG	denotes	decreased
T37	1234-1238	GENE	denotes	FLCN
T38	1239-1249	MPA	denotes	expression
T39	1275-1282	VAR	denotes	mutated
T40	1283-1302	GENE	denotes	folliculin proteins
T41	1283-1293	GENE	denotes	folliculin
T42	1313-1317	REG	denotes	risk
T43	1360-1364	DISEASE	denotes	BHDS
T44	1366-1383	DISEASE	denotes	fibrofolliculomas
T45	1385-1395	DISEASE	denotes	lung cysts
T46	1401-1414	DISEASE	denotes	tumorigenesis
T47	1492-1496	GENE	denotes	FLCN
T48	1502-1507	DISEASE	denotes	tumor
R0	T5	T4	ThemeOf	protein,mutated
R1	T7	T10	ThemeOf	Birt-Hogg-Dubé syndrome,caused
R2	T8	T10	ThemeOf	BHDS,caused
R3	T11	T10	CauseOf	mutation,caused
R4	T12	T11	ThemeOf	folliculin,mutation
R5	T13	T11	ThemeOf	FLCN,mutation
R6	T15	T14	ThemeOf	folliculin proteins,mutant
R7	T15	T18	ThemeOf	folliculin proteins,mutations
R8	T17	T18	ThemeOf	FLCN,mutations
R9	T18	T20	CauseOf	mutations,contribute
R10	T25	T30	CauseOf	deletion,cause
R11	T25	T31	CauseOf	deletion,lack
R12	T26	T25	ThemeOf	FLCN,deletion
R13	T26	T27	ThemeOf	FLCN,hit
R14	T27	T30	CauseOf	hit,cause
R15	T27	T31	CauseOf	hit,lack
R16	T28	T25	ThemeOf	FLCN,deletion
R17	T28	T27	ThemeOf	FLCN,hit
R18	T32	T31	ThemeOf	folliculin protein,lack
R19	T36	T42	CauseOf	decreased,risk
R20	T37	T38	ThemeOf	FLCN,expression
R21	T38	T36	ThemeOf	expression,decreased
R22	T40	T39	ThemeOf	folliculin proteins,mutated
R23	T40	T42	ThemeOf	folliculin proteins,risk
R24	T43	T42	ThemeOf	BHDS,risk
R25	T44	T42	ThemeOf	fibrofolliculomas,risk
R26	T45	T42	ThemeOf	lung cysts,risk
R27	T46	T42	ThemeOf	tumorigenesis,risk