PubMed:10581038 / 1111-1327 JSON TXT

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Id	Subject	Object	Predicate	Lexical cue
T320	8-20	CHEBI:47885	denotes	dinucleotide
T321	21-27	SO:0001068	denotes	repeat
T322	70-85	GO:0006298	denotes	mismatch repair
T324	93-96	CHEBI:16768	denotes	MSH
T328	93-96	D009074	denotes	MSH
T329	93-96	D009074	denotes	MSH
T330	93-97	PR:000010666	denotes	MSH2
T331	93-97	PR:P25847	denotes	MSH2
T332	93-97	PR:P43246	denotes	MSH2
T333	93-97	P22711	denotes	MSH2
T334	93-97	PR:P22711	denotes	MSH2
T335	93-97	PR:P54275	denotes	MSH2
T336	93-97	PR:O74773	denotes	MSH2
T337	93-97	PR:P43247	denotes	MSH2
T338	93-97	PR:Q553L4	denotes	MSH2
T339	93-97	PR:O24617	denotes	MSH2
T340	144-147	CVCL_D569	denotes	CAG
T341	148-154	SO:0001068	denotes	repeat
T342	167-177	SO:0000781	denotes	transgenic
T343	167-182	10090	denotes	transgenic mice
T344	167-182	D008822	denotes	transgenic mice
T345	178-182	PR:000005054	denotes	mice
T347	178-182	O89094	denotes	mice
T350	192-196	SO:0000147	denotes	exon
T349	192-196	PR:P33696	denotes	exon
T351	202-207	D006801	denotes	human

Id	Subject	Object	Predicate	Lexical cue
T9	0-216	DRI_Challenge	denotes	Because dinucleotide repeat instability is known to increase when the mismatch repair enzyme MSH2 is missing, we examined instability of the HD CAG repeat by crossing transgenic mice carrying exon 1 of human HD (ref.

Id	Subject	Object	Predicate	Lexical cue
T0	93-97	gene:4436	denotes	MSH2
T1	141-143	disease:C0020179	denotes	HD
T2	93-97	gene:4436	denotes	MSH2
T3	208-210	disease:C0020179	denotes	HD
R1	T0	T1	associated_with	MSH2,HD
R2	T2	T3	associated_with	MSH2,HD