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PMC:1584416 / 72-282 JSONTXT

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craft-sa-dev

Id Subject Object Predicate Lexical cue
T96 53-61 IN denotes Although
T97 153-155 VBZ denotes is
T98 62-70 NN denotes compound
T99 71-85 NN denotes heterozygosity
T100 85-87 , denotes ,
T101 87-89 CC denotes or
T102 90-93 DT denotes the
T103 94-102 NN denotes presence
T104 103-105 IN denotes of
T105 106-109 CD denotes two
T106 127-134 NNS denotes alleles
T107 110-119 JJ denotes different
T108 120-126 JJ denotes mutant
T109 135-137 IN denotes of
T110 138-141 DT denotes the
T111 147-151 NN denotes gene
T112 142-146 JJ denotes same
T113 151-153 , denotes ,
T115 156-162 JJ denotes common
T116 163-165 IN denotes in
T117 166-171 JJ denotes human
T118 182-189 NN denotes disease
T119 172-181 JJ denotes recessive
T120 189-191 , denotes ,
T121 191-194 PRP$ denotes its
T122 195-204 NN denotes potential
T123 205-207 TO denotes to
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

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 127-134 SO:0001023 denotes alleles
T23 147-151 SO:0000704 denotes gene
T24 166-171 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 120-126 SO_EXT:sequence_altered_entity_or_alteration_process denotes mutant
T52 127-134 SO_EXT:0001023 denotes alleles
T53 147-151 SO_EXT:0000704 denotes gene
T54 166-171 NCBITaxon:9606 denotes human