PMC:1435744 / 4727-4982
Annnotations
craft-ca-core-ex-dev
Below, discontinuous spans are shown in the chain model. You can change it to the bag model.
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3477 | 14-23 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutations |
| T3478 | 27-32 | NCBITaxon:9606 | denotes | human |
| T3479 | 33-36 | PR_EXT:000005904 | denotes | CRX |
| T3480 | 97-110 | CL:0000210 | denotes | photoreceptor |
| T3481 | 121-130 | GO:0030849 | denotes | autosomal |
| T3482 | 140-144 | CL:0000573 | denotes | cone |
| T3483 | 145-148 | CL:0000604 | denotes | rod |
| T3484 | 162-171 | GO:0030849 | denotes | autosomal |
craft-ca-core-dev
Below, discontinuous spans are shown in the chain model. You can change it to the bag model.
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3283 | 27-32 | NCBITaxon:9606 | denotes | human |
| T3284 | 33-36 | PR:000005904 | denotes | CRX |
| T3285 | 97-110 | CL:0000210 | denotes | photoreceptor |
| T3286 | 121-130 | GO:0030849 | denotes | autosomal |
| T3287 | 140-144 | CL:0000573 | denotes | cone |
| T3288 | 145-148 | CL:0000604 | denotes | rod |
| T3289 | 162-171 | GO:0030849 | denotes | autosomal |
craft-sa-dev
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T4046 | 0-255 | sentence | denotes | In addition, mutations of human CRX have been demonstrated to be associated with three types of photoreceptor diseases: autosomal dominant cone-rod dystrophy 2, autosomal dominant-type retinitis pigmentosa, and Leber's congenital amaurosis (LCA) [11-14]. |
| T4047 | 1-3 | IN | denotes | In |
| T4048 | 47-59 | VBN | denotes | demonstrated |
| T4049 | 4-12 | NN | denotes | addition |
| T4050 | 12-14 | , | denotes | , |
| T4051 | 14-23 | NNS | denotes | mutations |
| T4052 | 24-26 | IN | denotes | of |
| T4053 | 27-32 | JJ | denotes | human |
| T4054 | 33-36 | NN | denotes | CRX |
| T4055 | 37-41 | VBP | denotes | have |
| T4056 | 42-46 | VBN | denotes | been |
| T4057 | 60-62 | TO | denotes | to |
| T4058 | 66-76 | VBN | denotes | associated |
| T4059 | 63-65 | VB | denotes | be |
| T4060 | 77-81 | IN | denotes | with |
| T4061 | 82-87 | CD | denotes | three |
| T4062 | 88-93 | NNS | denotes | types |
| T4063 | 94-96 | IN | denotes | of |
| T4064 | 97-110 | NN | denotes | photoreceptor |
| T4065 | 111-119 | NNS | denotes | diseases |
| T4066 | 119-121 | : | denotes | : |
| T4067 | 121-130 | JJ | denotes | autosomal |
| T4068 | 131-139 | JJ | denotes | dominant |
| T4069 | 149-158 | NN | denotes | dystrophy |
| T4070 | 140-144 | NN | denotes | cone |
| T4071 | 145-148 | NN | denotes | rod |
| T4072 | 144-145 | HYPH | denotes | - |
| T4073 | 159-160 | CD | denotes | 2 |
| T4074 | 160-162 | , | denotes | , |
| T4075 | 162-171 | JJ | denotes | autosomal |
| T4076 | 172-180 | JJ | denotes | dominant |
| T4077 | 181-185 | NN | denotes | type |
| T4078 | 180-181 | HYPH | denotes | - |
| T4079 | 196-206 | NN | denotes | pigmentosa |
| T4080 | 186-195 | NN | denotes | retinitis |
| T4081 | 206-208 | , | denotes | , |
| T4082 | 208-211 | CC | denotes | and |
| T4083 | 212-217 | NNP | denotes | Leber |
| T4084 | 231-240 | NN | denotes | amaurosis |
| T4085 | 217-219 | POS | denotes | 's |
| T4086 | 220-230 | JJ | denotes | congenital |
| T4087 | 241-242 | -LRB- | denotes | ( |
| T4088 | 242-245 | NN | denotes | LCA |
| T4089 | 245-246 | -RRB- | denotes | ) |
| T4090 | 247-248 | -LRB- | denotes | [ |
| T4091 | 248-250 | CD | denotes | 11 |
| T4092 | 250-251 | SYM | denotes | - |
| T4093 | 251-253 | CD | denotes | 14 |
| T4094 | 253-254 | -RRB- | denotes | ] |
| T4095 | 254-255 | . | denotes | . |
| R788 | T4053 | T4054 | amod | human,CRX |
| R794 | T4054 | T4052 | pobj | CRX,of |
| R797 | T4055 | T4048 | aux | have,demonstrated |
| R800 | T4056 | T4048 | auxpass | been,demonstrated |
| R805 | T4057 | T4058 | aux | to,associated |
| R808 | T4058 | T4048 | xcomp | associated,demonstrated |
| R816 | T4059 | T4058 | auxpass | be,associated |
| R820 | T4060 | T4058 | prep | with,associated |
| R824 | T4061 | T4062 | nummod | three,types |
| R828 | T4062 | T4060 | pobj | types,with |
| R830 | T4063 | T4062 | prep | of,types |
| R831 | T4047 | T4048 | prep | In,demonstrated |
| R832 | T4049 | T4047 | pobj | addition,In |
| R833 | T4050 | T4048 | punct | ", ",demonstrated |
| R834 | T4064 | T4065 | compound | photoreceptor,diseases |
| R835 | T4051 | T4048 | nsubjpass | mutations,demonstrated |
| R836 | T4052 | T4051 | prep | of,mutations |
| R837 | T4065 | T4063 | pobj | diseases,of |
| R838 | T4066 | T4062 | punct | : ,types |
| R839 | T4067 | T4068 | amod | autosomal,dominant |
| R840 | T4068 | T4069 | amod | dominant,dystrophy |
| R841 | T4069 | T4062 | appos | dystrophy,types |
| R844 | T4070 | T4071 | compound | cone,rod |
| R847 | T4071 | T4069 | compound | rod,dystrophy |
| R850 | T4072 | T4071 | punct | -,rod |
| R854 | T4073 | T4069 | nummod | 2,dystrophy |
| R856 | T4074 | T4069 | punct | ", ",dystrophy |
| R859 | T4075 | T4076 | amod | autosomal,dominant |
| R866 | T4076 | T4077 | amod | dominant,type |
| R871 | T4077 | T4079 | compound | type,pigmentosa |
| R875 | T4078 | T4077 | punct | -,type |
| R878 | T4079 | T4069 | conj | pigmentosa,dystrophy |
| R883 | T4080 | T4079 | compound | retinitis,pigmentosa |
| R886 | T4081 | T4079 | punct | ", ",pigmentosa |
| R890 | T4082 | T4079 | cc | and,pigmentosa |
| R894 | T4083 | T4084 | poss | Leber,amaurosis |
| R898 | T4084 | T4079 | conj | amaurosis,pigmentosa |
| R901 | T4085 | T4083 | case | 's,Leber |
| R905 | T4086 | T4084 | amod | congenital,amaurosis |
| R907 | T4087 | T4084 | punct | (,amaurosis |
| R912 | T4088 | T4084 | appos | LCA,amaurosis |
| R919 | T4089 | T4048 | punct | ),demonstrated |
| R923 | T4090 | T4091 | punct | [,11 |
| R927 | T4091 | T4048 | parataxis | 11,demonstrated |
| R931 | T4092 | T4093 | punct | -,14 |
| R935 | T4093 | T4091 | prep | 14,11 |
| R938 | T4094 | T4091 | punct | ],11 |
| R943 | T4095 | T4048 | punct | .,demonstrated |