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PMC:1584416 / 152-444 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T97 73-75 VBZ denotes is
T100 5-7 , denotes ,
T101 7-9 CC denotes or
T102 10-13 DT denotes the
T103 14-22 NN denotes presence
T104 23-25 IN denotes of
T105 26-29 CD denotes two
T106 47-54 NNS denotes alleles
T107 30-39 JJ denotes different
T108 40-46 JJ denotes mutant
T109 55-57 IN denotes of
T110 58-61 DT denotes the
T111 67-71 NN denotes gene
T112 62-66 JJ denotes same
T113 71-73 , denotes ,
T114 169-179 VBN denotes documented
T115 76-82 JJ denotes common
T116 83-85 IN denotes in
T117 86-91 JJ denotes human
T118 102-109 NN denotes disease
T119 92-101 JJ denotes recessive
T120 109-111 , denotes ,
T121 111-114 PRP$ denotes its
T122 115-124 NN denotes potential
T123 125-127 TO denotes to
T124 128-134 VB denotes impact
T125 135-142 NN denotes disease
T126 143-150 NN denotes outcome
T127 151-154 VBZ denotes has
T128 155-158 RB denotes not
T129 159-163 VBN denotes been
T130 164-168 RB denotes well
T131 179-180 . denotes .
T133 181-185 DT denotes This
T134 186-188 VBZ denotes is
T135 189-193 RBS denotes most
T136 194-200 RB denotes likely
T137 201-208 IN denotes because
T138 209-211 IN denotes of
T139 212-215 DT denotes the
T140 225-235 NN denotes difficulty
T141 216-224 JJ denotes inherent
T142 236-238 IN denotes in
T143 239-253 VBG denotes distinguishing
T144 254-262 JJ denotes specific
T145 273-280 NNS denotes effects
T146 263-272 JJ denotes biallelic
T147 281-285 IN denotes from
R11 T97 T114 advcl is,documented
R16 T102 T103 det the,presence
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
R56 T145 T143 dobj effects,distinguishing
R57 T146 T145 amod biallelic,effects
R34 T121 T122 poss its,potential
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
R53 T142 T140 prep in,difficulty
R54 T143 T142 pcomp distinguishing,in
R55 T144 T145 amod specific,effects
R58 T147 T143 prep from,distinguishing

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 47-54 SO:0001023 denotes alleles
T23 67-71 SO:0000704 denotes gene
T24 86-91 NCBITaxon:9606 denotes human
T25 265-272 SO:0001023 denotes allelic

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 40-46 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T52 47-54 SO_EXT:0001023 denotes alleles
T53 67-71 SO_EXT:0000704 denotes gene
T54 86-91 NCBITaxon:9606 denotes human
T55 265-272 SO_EXT:0001023 denotes allelic