PMC:1584416 / 98-389
Annnotations
craft-sa-dev
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T95 | 26-234 | sentence | denotes | Although compound heterozygosity, or the presence of two different mutant alleles of the same gene, is common in human recessive disease, its potential to impact disease outcome has not been well documented. |
| T96 | 27-35 | IN | denotes | Although |
| T97 | 127-129 | VBZ | denotes | is |
| T98 | 36-44 | NN | denotes | compound |
| T99 | 45-59 | NN | denotes | heterozygosity |
| T100 | 59-61 | , | denotes | , |
| T101 | 61-63 | CC | denotes | or |
| T102 | 64-67 | DT | denotes | the |
| T103 | 68-76 | NN | denotes | presence |
| T104 | 77-79 | IN | denotes | of |
| T105 | 80-83 | CD | denotes | two |
| T106 | 101-108 | NNS | denotes | alleles |
| T107 | 84-93 | JJ | denotes | different |
| T108 | 94-100 | JJ | denotes | mutant |
| T109 | 109-111 | IN | denotes | of |
| T110 | 112-115 | DT | denotes | the |
| T111 | 121-125 | NN | denotes | gene |
| T112 | 116-120 | JJ | denotes | same |
| T113 | 125-127 | , | denotes | , |
| T114 | 223-233 | VBN | denotes | documented |
| T115 | 130-136 | JJ | denotes | common |
| T116 | 137-139 | IN | denotes | in |
| T117 | 140-145 | JJ | denotes | human |
| T118 | 156-163 | NN | denotes | disease |
| T119 | 146-155 | JJ | denotes | recessive |
| T120 | 163-165 | , | denotes | , |
| T121 | 165-168 | PRP$ | denotes | its |
| T122 | 169-178 | NN | denotes | potential |
| T123 | 179-181 | TO | denotes | to |
| T124 | 182-188 | VB | denotes | impact |
| T125 | 189-196 | NN | denotes | disease |
| T126 | 197-204 | NN | denotes | outcome |
| T127 | 205-208 | VBZ | denotes | has |
| T128 | 209-212 | RB | denotes | not |
| T129 | 213-217 | VBN | denotes | been |
| T130 | 218-222 | RB | denotes | well |
| T131 | 233-234 | . | denotes | . |
| T133 | 235-239 | DT | denotes | This |
| T134 | 240-242 | VBZ | denotes | is |
| T135 | 243-247 | RBS | denotes | most |
| T136 | 248-254 | RB | denotes | likely |
| T137 | 255-262 | IN | denotes | because |
| T138 | 263-265 | IN | denotes | of |
| T139 | 266-269 | DT | denotes | the |
| T140 | 279-289 | NN | denotes | difficulty |
| T141 | 270-278 | JJ | denotes | inherent |
| R11 | T97 | T114 | advcl | is,documented |
| R12 | T98 | T99 | compound | compound,heterozygosity |
| R13 | T99 | T97 | nsubj | heterozygosity,is |
| R14 | T100 | T99 | punct | ", ",heterozygosity |
| R15 | T101 | T99 | cc | or,heterozygosity |
| R16 | T102 | T103 | det | the,presence |
| R17 | T103 | T99 | conj | presence,heterozygosity |
| R18 | T104 | T103 | prep | of,presence |
| R19 | T105 | T106 | nummod | two,alleles |
| R20 | T106 | T104 | pobj | alleles,of |
| R21 | T107 | T106 | amod | different,alleles |
| R22 | T108 | T106 | amod | mutant,alleles |
| R23 | T109 | T106 | prep | of,alleles |
| R24 | T110 | T111 | det | the,gene |
| R26 | T112 | T111 | amod | same,gene |
| R27 | T113 | T97 | punct | ", ",is |
| R31 | T118 | T116 | pobj | disease,in |
| R32 | T119 | T118 | amod | recessive,disease |
| R51 | T140 | T137 | pobj | difficulty,because |
| R52 | T141 | T140 | amod | inherent,difficulty |
| R34 | T121 | T122 | poss | its,potential |
| R10 | T96 | T97 | mark | Although,is |
| R25 | T111 | T109 | pobj | gene,of |
| R28 | T115 | T97 | acomp | common,is |
| R29 | T116 | T97 | prep | in,is |
| R30 | T117 | T118 | amod | human,disease |
| R33 | T120 | T114 | punct | ", ",documented |
| R35 | T122 | T114 | nsubjpass | potential,documented |
| R36 | T123 | T124 | aux | to,impact |
| R37 | T124 | T122 | acl | impact,potential |
| R38 | T125 | T126 | compound | disease,outcome |
| R39 | T126 | T124 | dobj | outcome,impact |
| R40 | T127 | T114 | aux | has,documented |
| R41 | T128 | T114 | neg | not,documented |
| R42 | T129 | T114 | auxpass | been,documented |
| R43 | T130 | T114 | advmod | well,documented |
| R44 | T131 | T114 | punct | .,documented |
| R45 | T133 | T134 | nsubj | This,is |
| R46 | T135 | T136 | advmod | most,likely |
| R47 | T136 | T137 | advmod | likely,because |
| R48 | T137 | T134 | prep | because,is |
| R49 | T138 | T137 | pcomp | of,because |
| R50 | T139 | T140 | det | the,difficulty |
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 |
|---|---|---|---|---|
| T22 | 101-108 | SO:0001023 | denotes | alleles |
| T23 | 121-125 | SO:0000704 | denotes | gene |
| T24 | 140-145 | NCBITaxon:9606 | denotes | human |
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 |
|---|---|---|---|---|
| T51 | 94-100 | SO_EXT:sequence_altered_entity_or_alteration_process | denotes | mutant |
| T52 | 101-108 | SO_EXT:0001023 | denotes | alleles |
| T53 | 121-125 | SO_EXT:0000704 | denotes | gene |
| T54 | 140-145 | NCBITaxon:9606 | denotes | human |