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PMC:1584416 / 80-372 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T95 44-252 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 45-53 IN denotes Although
T97 145-147 VBZ denotes is
T98 54-62 NN denotes compound
T99 63-77 NN denotes heterozygosity
T100 77-79 , denotes ,
T101 79-81 CC denotes or
T102 82-85 DT denotes the
T103 86-94 NN denotes presence
T104 95-97 IN denotes of
T105 98-101 CD denotes two
T106 119-126 NNS denotes alleles
T107 102-111 JJ denotes different
T108 112-118 JJ denotes mutant
T109 127-129 IN denotes of
T110 130-133 DT denotes the
T111 139-143 NN denotes gene
T112 134-138 JJ denotes same
T113 143-145 , denotes ,
T114 241-251 VBN denotes documented
T115 148-154 JJ denotes common
T116 155-157 IN denotes in
T117 158-163 JJ denotes human
T118 174-181 NN denotes disease
T119 164-173 JJ denotes recessive
T120 181-183 , denotes ,
T121 183-186 PRP$ denotes its
T122 187-196 NN denotes potential
T123 197-199 TO denotes to
T124 200-206 VB denotes impact
T125 207-214 NN denotes disease
T126 215-222 NN denotes outcome
T127 223-226 VBZ denotes has
T128 227-230 RB denotes not
T129 231-235 VBN denotes been
T130 236-240 RB denotes well
T131 251-252 . denotes .
T133 253-257 DT denotes This
T134 258-260 VBZ denotes is
T135 261-265 RBS denotes most
T136 266-272 RB denotes likely
T137 273-280 IN denotes because
T138 281-283 IN denotes of
T139 284-287 DT denotes the
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
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

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 119-126 SO:0001023 denotes alleles
T23 139-143 SO:0000704 denotes gene
T24 158-163 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 112-118 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T52 119-126 SO_EXT:0001023 denotes alleles
T53 139-143 SO_EXT:0000704 denotes gene
T54 158-163 NCBITaxon:9606 denotes human