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PMC:1584416 / 79-335 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T95 45-253 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 46-54 IN denotes Although
T97 146-148 VBZ denotes is
T98 55-63 NN denotes compound
T99 64-78 NN denotes heterozygosity
T100 78-80 , denotes ,
T101 80-82 CC denotes or
T102 83-86 DT denotes the
T103 87-95 NN denotes presence
T104 96-98 IN denotes of
T105 99-102 CD denotes two
T106 120-127 NNS denotes alleles
T107 103-112 JJ denotes different
T108 113-119 JJ denotes mutant
T109 128-130 IN denotes of
T110 131-134 DT denotes the
T111 140-144 NN denotes gene
T112 135-139 JJ denotes same
T113 144-146 , denotes ,
T114 242-252 VBN denotes documented
T115 149-155 JJ denotes common
T116 156-158 IN denotes in
T117 159-164 JJ denotes human
T118 175-182 NN denotes disease
T119 165-174 JJ denotes recessive
T120 182-184 , denotes ,
T121 184-187 PRP$ denotes its
T122 188-197 NN denotes potential
T123 198-200 TO denotes to
T124 201-207 VB denotes impact
T125 208-215 NN denotes disease
T126 216-223 NN denotes outcome
T127 224-227 VBZ denotes has
T128 228-231 RB denotes not
T129 232-236 VBN denotes been
T130 237-241 RB denotes well
T131 252-253 . denotes .
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
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

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 120-127 SO:0001023 denotes alleles
T23 140-144 SO:0000704 denotes gene
T24 159-164 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 113-119 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T52 120-127 SO_EXT:0001023 denotes alleles
T53 140-144 SO_EXT:0000704 denotes gene
T54 159-164 NCBITaxon:9606 denotes human