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PMC:1584416 / 98-389 JSONTXT

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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