
PubMed:11063736
Annnotations
c_corpus
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 14-20 | UBERON:0000922 | denotes | embryo |
T2 | 36-39 | CVCL_D569 | denotes | CAG |
T3 | 55-65 | SO:0000781 | denotes | transgenic |
T4 | 55-70 | 10090 | denotes | transgenic mice |
T5 | 55-70 | D008822 | denotes | transgenic mice |
T6 | 66-70 | PR:000005054 | denotes | mice |
T8 | 66-70 | O89094 | denotes | mice |
T14 | 84-104 | D006816 | denotes | Huntington's disease |
T15 | 84-104 | D006816 | denotes | Huntington's disease |
T18 | 105-109 | SO:0000704 | denotes | gene |
T19 | 160-173 | CHEBI:74953 | denotes | trinucleotide |
T20 | 185-190 | D006801 | denotes | human |
T21 | 191-198 | D004194 | denotes | disease |
T22 | 191-198 | D004194 | denotes | disease |
T23 | 277-290 | CHEBI:74953 | denotes | trinucleotide |
T24 | 277-307 | SO:0002165 | denotes | trinucleotide repeat expansion |
T26 | 377-380 | CVCL_D569 | denotes | CAG |
T27 | 381-394 | CHEBI:74953 | denotes | trinucleotide |
T28 | 395-401 | SO:0001068 | denotes | repeat |
T29 | 407-416 | SO:0000902 | denotes | transgene |
T31 | 432-436 | SO:0000147 | denotes | exon |
T30 | 432-436 | PR:P33696 | denotes | exon |
T32 | 454-459 | D006801 | denotes | human |
T37 | 460-480 | D006816 | denotes | Huntington's disease |
T38 | 460-480 | D006816 | denotes | Huntington's disease |
T41 | 486-490 | SO:0000704 | denotes | gene |
T42 | 515-520 | 10090 | denotes | mouse |
T43 | 515-520 | D051379 | denotes | mouse |
T44 | 568-572 | UBERON:0003101 | denotes | male |
T45 | 568-572 | CHEBI:30780 | denotes | male |
T46 | 615-618 | CVCL_D569 | denotes | CAG |
T47 | 619-625 | SO:0001068 | denotes | repeat |
T48 | 645-650 | D006801 | denotes | human |
T49 | 654-658 | SO:0000704 | denotes | gene |
T51 | 675-679 | CHEBI:30780 | denotes | male |
T50 | 675-679 | UBERON:0003101 | denotes | male |
T52 | 684-690 | UBERON:0003100 | denotes | female |
T53 | 754-760 | SO:0001068 | denotes | repeat |
T54 | 804-810 | SO:0001068 | denotes | repeat |
T55 | 865-868 | CVCL_D569 | denotes | CAG |
T56 | 914-920 | UBERON:0000922 | denotes | embryo |
T58 | 1035-1038 | CHEBI:16991 | denotes | DNA |
T60 | 1035-1038 | D004247 | denotes | DNA |
T59 | 1035-1038 | SO:0000352 | denotes | DNA |
T57 | 1035-1038 | GO:0005574 | denotes | DNA |
T61 | 1046-1052 | UBERON:0000922 | denotes | embryo |
T62 | 1079-1085 | UBERON:0000922 | denotes | embryo |
T63 | 1138-1145 | D004194 | denotes | disease |
T64 | 1138-1145 | D004194 | denotes | disease |
UseCases_ArguminSci_Discourse
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-110 | DRI_Outcome | denotes | Gender of the embryo contributes to CAG instability in transgenic mice containing a Huntington's disease gene. |
T2 | 111-199 | DRI_Background | denotes | Gender is known to influence the transmission of trinucleotide repeats in human disease. |
T3 | 200-321 | DRI_Approach | denotes | However, the molecular basis for the parent-of-origin effect associated with trinucleotide repeat expansion is not known. |
T4 | 322-491 | DRI_Approach | denotes | We have followed, during transmission, the fate of the CAG trinucleotide repeat in a transgene containing the exon 1 portion of the human Huntington's disease (HD) gene. |
T5 | 492-583 | DRI_Background | denotes | Similar to humans, the mouse transmits expansions predominantly through the male germ line. |
T6 | 584-722 | DRI_Outcome | denotes | Surprisingly, we find that the CAG repeat size of the mutant human HD gene is different in male and female progeny from identical fathers. |
T7 | 723-811 | DRI_Approach | denotes | Males predominantly expand the repeat whereas females predominantly contract the repeat. |
T8 | 812-921 | DRI_Approach | denotes | In contrast to the classic definition of imprinting, CAG expansion is influenced by the gender of the embryo. |
T9 | 922-1053 | DRI_Outcome | denotes | Our results raise the possibility that there are X- or Y-encoded factors that influence repair or replication of DNA in the embryo. |
T10 | 1054-1189 | DRI_Background | denotes | Gender dependence in the embryo may explain why expansion in HD from premutation to disease primarily occurs through the paternal line. |