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PubMed:14510914 JSONTXT

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TEST-CellLine

Id Subject Object Predicate Lexical cue cellosaurus_accession_id
T1 1606-1611 CellLine denotes COS-7 CVCL_0224

TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism D003409
T2 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409
T3 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism D007037
T4 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism D007037
T5 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409

TEST-ChemicalEntity

Id Subject Object Predicate Lexical cue ID:
T1 55-68 ChemicalEntity denotes sodium/iodide D012974|http://purl.obolibrary.org/obo/CHEBI_33167
T3 99-105 ChemicalEntity denotes Iodide http://purl.obolibrary.org/obo/CHEBI_16382
T4 185-192 ChemicalEntity denotes thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T5 208-214 ChemicalEntity denotes iodide D007454|http://purl.obolibrary.org/obo/CHEBI_16382
T7 259-266 ChemicalEntity denotes thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T8 471-484 ChemicalEntity denotes sodium/iodide D012974|http://purl.obolibrary.org/obo/CHEBI_33167
T10 496-499 ChemicalEntity denotes NIS http://purl.obolibrary.org/obo/CHEBI_53204
T11 668-674 ChemicalEntity denotes iodide D007454|http://purl.obolibrary.org/obo/CHEBI_16382
T13 689-696 ChemicalEntity denotes thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T14 733-739 ChemicalEntity denotes iodide D007454|http://purl.obolibrary.org/obo/CHEBI_16382
T16 825-836 ChemicalEntity denotes L-thyroxine http://purl.obolibrary.org/obo/CHEBI_58448|http://purl.obolibrary.org/obo/CHEBI_18332
T18 864-871 ChemicalEntity denotes Thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T19 956-977 ChemicalEntity denotes recombinant human TSH D057073
T20 1054-1061 ChemicalEntity denotes thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T21 1162-1165 ChemicalEntity denotes NIS http://purl.obolibrary.org/obo/CHEBI_53204
T22 1680-1683 ChemicalEntity denotes NIS http://purl.obolibrary.org/obo/CHEBI_53204
T23 1706-1712 ChemicalEntity denotes iodide D007454|http://purl.obolibrary.org/obo/CHEBI_16382
T25 1911-1914 ChemicalEntity denotes NIS http://purl.obolibrary.org/obo/CHEBI_53204

TEST-OrganismTaxon

Id Subject Object Predicate Lexical cue
T1 502-509 OrganismTaxon denotes PATIENT
T2 968-973 OrganismTaxon denotes human
T3 1152-1161 OrganismTaxon denotes patient's
T4 1342-1349 OrganismTaxon denotes patient
T5 1783-1790 OrganismTaxon denotes patient

Test-SequenceVariant

Id Subject Object Predicate Lexical cue
T1 1201-1216 SequenceVariant denotes deletion of the

Test-GeneOrGeneProduct

Id Subject Object Predicate Lexical cue
T1 55-78 GeneOrGeneProduct denotes sodium/iodide symporter
T2 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T3 983-989 GeneOrGeneProduct denotes saliva
T4 1488-1497 GeneOrGeneProduct denotes a protein

Test-merged-2

Id Subject Object Predicate Lexical cue #label ID: cellosaurus_accession_id
T33877 1606-1611 CellLine denotes COS-7 CVCL_0224
T22428 1201-1216 SequenceVariant denotes deletion of the
T37045 55-68 ChemicalEntity denotes sodium/iodide D012974|http://purl.obolibrary.org/obo/CHEBI_33167
T38837 99-105 ChemicalEntity denotes Iodide http://purl.obolibrary.org/obo/CHEBI_16382
T20745 185-192 ChemicalEntity denotes thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T39002 208-214 ChemicalEntity denotes iodide D007454|http://purl.obolibrary.org/obo/CHEBI_16382
T7 259-266 ChemicalEntity denotes thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T8 471-484 ChemicalEntity denotes sodium/iodide D012974|http://purl.obolibrary.org/obo/CHEBI_33167
T10 496-499 ChemicalEntity denotes NIS http://purl.obolibrary.org/obo/CHEBI_53204
T11 668-674 ChemicalEntity denotes iodide D007454|http://purl.obolibrary.org/obo/CHEBI_16382
T13 689-696 ChemicalEntity denotes thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T14 733-739 ChemicalEntity denotes iodide D007454|http://purl.obolibrary.org/obo/CHEBI_16382
T16 825-836 ChemicalEntity denotes L-thyroxine http://purl.obolibrary.org/obo/CHEBI_58448|http://purl.obolibrary.org/obo/CHEBI_18332
T18 864-871 ChemicalEntity denotes Thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T19 956-977 ChemicalEntity denotes recombinant human TSH D057073
T20 1054-1061 ChemicalEntity denotes thyroid http://purl.obolibrary.org/obo/CHEBI_9584
T21 1162-1165 ChemicalEntity denotes NIS http://purl.obolibrary.org/obo/CHEBI_53204
T22 1680-1683 ChemicalEntity denotes NIS http://purl.obolibrary.org/obo/CHEBI_53204
T23 1706-1712 ChemicalEntity denotes iodide D007454|http://purl.obolibrary.org/obo/CHEBI_16382
T25 1911-1914 ChemicalEntity denotes NIS http://purl.obolibrary.org/obo/CHEBI_53204
T86897 55-78 GeneOrGeneProduct denotes sodium/iodide symporter
T89843 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T53423 983-989 GeneOrGeneProduct denotes saliva
T25351 1488-1497 GeneOrGeneProduct denotes a protein
T84818 502-509 OrganismTaxon denotes PATIENT
T17883 968-973 OrganismTaxon denotes human
T20753 1152-1161 OrganismTaxon denotes patient's
T69365 1342-1349 OrganismTaxon denotes patient
T59389 1783-1790 OrganismTaxon denotes patient
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism D003409
T2 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409
T3 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism D007037
T4 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism D007037
T5 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 307-332 HP_0000851 denotes congenital hypothyroidism
T2 318-332 HP_0000821 denotes hypothyroidism

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
14510914-0#55#78#gene6528 55-78 gene6528 denotes sodium/iodide symporter
14510914-0#0#25#diseaseC0010308 0-25 diseaseC0010308 denotes Congenital hypothyroidism
14510914-11#74#77#gene6528 1680-1683 gene6528 denotes NIS
14510914-11#165#168#diseaseC0271826 1771-1774 diseaseC0271826 denotes ITD
55#78#gene65280#25#diseaseC0010308 14510914-0#55#78#gene6528 14510914-0#0#25#diseaseC0010308 associated_with sodium/iodide symporter,Congenital hypothyroidism
74#77#gene6528165#168#diseaseC0271826 14510914-11#74#77#gene6528 14510914-11#165#168#diseaseC0271826 associated_with NIS,ITD

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 0-25 HP:0000851 denotes Congenital hypothyroidism
AB1 307-332 HP:0000851 denotes congenital hypothyroidism
AB2 536-550 HP:0000821 denotes hypothyroidism
AB3 764-778 HP:0000821 denotes hypothyroidism
AB4 1856-1881 HP:0000851 denotes congenital hypothyroidism

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 1666-1679 DNAMutation:c|DEL|-443_-439| denotes del-(439-443)

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1680-1683 gene:6528 denotes NIS
T1 1771-1774 disease:C0271826 denotes ITD
T2 1911-1914 gene:6528 denotes NIS
T3 1856-1881 disease:C0010308 denotes congenital hypothyroidism
T4 1911-1914 gene:6528 denotes NIS
T5 1856-1881 disease:C0342200 denotes congenital hypothyroidism
R1 T0 T1 associated_with NIS,ITD
R2 T2 T3 associated_with NIS,congenital hypothyroidism
R3 T4 T5 associated_with NIS,congenital hypothyroidism

biored-valid-deepseek-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T3 124-127 DiseaseOrPhenotypicFeature denotes ITD
T4 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T5 471-500 GeneOrGeneProduct denotes sodium/iodide symporter (NIS)
T6 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T7 605-608 DiseaseOrPhenotypicFeature denotes ITD
T8 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T9 825-836 ChemicalEntity denotes L-thyroxine
T10 956-977 ChemicalEntity denotes recombinant human TSH
T11 1162-1165 GeneOrGeneProduct denotes NIS
T12 1524-1535 ChemicalEntity denotes amino acids
T13 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism

biored-valid

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-78 GeneOrGeneProduct denotes sodium/iodide symporter
T3 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T4 124-127 DiseaseOrPhenotypicFeature denotes ITD
T5 168-192 DiseaseOrPhenotypicFeature denotes inability of the thyroid
T6 208-214 ChemicalEntity denotes iodide
T7 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T8 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T9 496-499 GeneOrGeneProduct denotes NIS
T10 502-509 OrganismTaxon denotes PATIENT
T11 525-530 OrganismTaxon denotes woman
T12 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T13 605-608 DiseaseOrPhenotypicFeature denotes ITD
T14 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T15 668-674 ChemicalEntity denotes iodide
T16 733-739 ChemicalEntity denotes iodide
T17 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism
T18 825-836 ChemicalEntity denotes L-thyroxine
T19 872-883 ChemicalEntity denotes radioiodide
T20 968-973 OrganismTaxon denotes human
T21 974-977 GeneOrGeneProduct denotes TSH
T22 1000-1002 ChemicalEntity denotes I-
T23 1083-1085 ChemicalEntity denotes I-
T24 1152-1159 OrganismTaxon denotes patient
T25 1162-1165 GeneOrGeneProduct denotes NIS
T26 1201-1258 SequenceVariant denotes deletion of the coding sequence (nt 1314 through nt 1328)
T27 1267-1310 SequenceVariant denotes insertion of 15 nt duplicating the first 15
T28 1342-1349 OrganismTaxon denotes patient
T29 1498-1556 SequenceVariant denotes lacking the five terminal amino acids of exon XI (439-443)
T30 1606-1611 CellLine denotes COS-7
T31 1666-1679 SequenceVariant denotes del-(439-443)
T32 1680-1683 GeneOrGeneProduct denotes NIS
T33 1706-1712 ChemicalEntity denotes iodide
T34 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T35 1783-1790 OrganismTaxon denotes patient
T36 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T37 1911-1914 GeneOrGeneProduct denotes NIS

biored-valid-deepseek-nr-g

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-78 GeneOrGeneProduct denotes sodium/iodide symporter
T3 99-128 DiseaseOrPhenotypicFeature denotes Iodide transport defect (ITD)
T4 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T5 471-500 GeneOrGeneProduct denotes sodium/iodide symporter (NIS)
T6 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T7 605-608 DiseaseOrPhenotypicFeature denotes ITD
T8 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T9 725-727 SequenceVariant denotes nt
T10 825-836 ChemicalEntity denotes L-thyroxine
T11 872-883 ChemicalEntity denotes radioiodide
T12 965-967 SequenceVariant denotes nt
T13 974-977 GeneOrGeneProduct denotes TSH
T14 1000-1002 ChemicalEntity denotes I-
T15 1162-1165 GeneOrGeneProduct denotes NIS
T16 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism

biored-valid-deepseek-r-ng

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-78 GeneOrGeneProduct denotes sodium/iodide symporter
T3 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T4 124-127 DiseaseOrPhenotypicFeature denotes ITD
T5 208-214 ChemicalEntity denotes iodide
T6 496-499 GeneOrGeneProduct denotes NIS
T7 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T8 825-836 ChemicalEntity denotes L-thyroxine
T9 956-977 ChemicalEntity denotes recombinant human TSH
T10 1000-1002 ChemicalEntity denotes I-
T11 1162-1170 GeneOrGeneProduct denotes NIS gene
T12 1182-1209 SequenceVariant denotes 15 nucleotide (nt) deletion
T13 1267-1336 SequenceVariant denotes insertion of 15 nt duplicating the first 15 nt of the adjacent intron
T14 1606-1617 CellLine denotes COS-7 cells
T15 1666-1679 SequenceVariant denotes del-(439-443)

biored-valid-deepseek-r-g

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-78 GeneOrGeneProduct denotes sodium/iodide symporter
T3 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T4 124-127 DiseaseOrPhenotypicFeature denotes ITD
T5 208-214 ChemicalEntity denotes iodide
T6 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T7 478-484 ChemicalEntity denotes iodide
T8 496-499 GeneOrGeneProduct denotes NIS
T9 605-608 DiseaseOrPhenotypicFeature denotes ITD
T10 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T11 825-836 ChemicalEntity denotes L-thyroxine
T12 968-973 OrganismTaxon denotes human
T13 974-977 GeneOrGeneProduct denotes TSH
T14 1000-1002 ChemicalEntity denotes I-
T15 1182-1209 SequenceVariant denotes 15 nucleotide (nt) deletion
T16 1606-1617 CellLine denotes COS-7 cells
T17 1666-1683 SequenceVariant denotes del-(439-443) NIS

biored-valid-gemini-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T3 99-105 ChemicalEntity denotes Iodide
T4 106-128 DiseaseOrPhenotypicFeature denotes transport defect (ITD)
T5 134-147 DiseaseOrPhenotypicFeature denotes rare disorder
T6 208-214 ChemicalEntity denotes iodide
T7 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T8 471-500 GeneOrGeneProduct denotes sodium/iodide symporter (NIS)
T9 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T10 605-608 DiseaseOrPhenotypicFeature denotes ITD
T11 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T12 668-674 ChemicalEntity denotes iodide
T13 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism
T14 825-836 ChemicalEntity denotes L-thyroxine
T15 872-883 ChemicalEntity denotes radioiodide
T16 956-973 ChemicalEntity denotes recombinant human
T17 974-977 GeneOrGeneProduct denotes TSH
T18 1000-1002 ChemicalEntity denotes I-
T19 1152-1161 OrganismTaxon denotes patient's
T20 1162-1170 GeneOrGeneProduct denotes NIS gene
T21 1182-1209 SequenceVariant denotes 15 nucleotide (nt) deletion
T22 1267-1276 SequenceVariant denotes insertion
T23 1374-1392 SequenceVariant denotes insertion/deletion
T24 1490-1497 GeneOrGeneProduct denotes protein
T25 1606-1611 CellLine denotes COS-7
T26 1666-1683 GeneOrGeneProduct denotes del-(439-443) NIS
T27 1706-1712 ChemicalEntity denotes iodide
T28 1734-1742 SequenceVariant denotes mutation
T29 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T30 1783-1790 OrganismTaxon denotes patient
T31 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T32 1895-1903 SequenceVariant denotes deletion
T33 1911-1919 GeneOrGeneProduct denotes NIS gene

biored-valid-gemini-r-ng

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 39-47 SequenceVariant denotes deletion
T3 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T4 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T5 124-127 DiseaseOrPhenotypicFeature denotes ITD
T6 208-214 ChemicalEntity denotes iodide
T7 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T8 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T9 496-499 GeneOrGeneProduct denotes NIS
T10 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T11 605-608 DiseaseOrPhenotypicFeature denotes ITD
T12 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T13 668-674 ChemicalEntity denotes iodide
T14 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism
T15 825-836 ChemicalEntity denotes L-thyroxine
T16 872-883 ChemicalEntity denotes radioiodide
T17 956-977 GeneOrGeneProduct denotes recombinant human TSH
T18 1000-1002 ChemicalEntity denotes I-
T19 1162-1170 GeneOrGeneProduct denotes NIS gene
T20 1182-1209 SequenceVariant denotes 15 nucleotide (nt) deletion
T21 1267-1285 SequenceVariant denotes insertion of 15 nt
T22 1374-1392 SequenceVariant denotes insertion/deletion
T23 1452-1460 SequenceVariant denotes deletion
T24 1606-1617 CellLine denotes COS-7 cells
T25 1666-1679 SequenceVariant denotes del-(439-443)
T26 1706-1712 ChemicalEntity denotes iodide
T27 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T28 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T29 1911-1919 GeneOrGeneProduct denotes NIS gene

biored-valid-gemini-r-g

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 39-47 SequenceVariant denotes deletion
T3 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T4 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T5 124-127 DiseaseOrPhenotypicFeature denotes ITD
T6 208-214 ChemicalEntity denotes iodide
T7 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T8 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T9 496-499 GeneOrGeneProduct denotes NIS
T10 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T11 605-608 DiseaseOrPhenotypicFeature denotes ITD
T12 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T13 668-674 ChemicalEntity denotes iodide
T14 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism
T15 825-836 ChemicalEntity denotes L-thyroxine
T16 968-973 OrganismTaxon denotes human
T17 974-977 GeneOrGeneProduct denotes TSH
T18 1000-1002 ChemicalEntity denotes I-
T19 1162-1165 GeneOrGeneProduct denotes NIS
T20 1201-1209 SequenceVariant denotes deletion
T21 1267-1276 SequenceVariant denotes insertion
T22 1374-1392 SequenceVariant denotes insertion/deletion
T23 1452-1460 SequenceVariant denotes deletion
T24 1606-1611 CellLine denotes COS-7
T25 1666-1679 SequenceVariant denotes del-(439-443)
T26 1680-1683 GeneOrGeneProduct denotes NIS
T27 1706-1712 ChemicalEntity denotes iodide
T28 1734-1742 SequenceVariant denotes mutation
T29 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T30 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism

biored-valid-gpt-nr-ng

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T3 99-128 DiseaseOrPhenotypicFeature denotes Iodide transport defect (ITD)
T4 471-500 GeneOrGeneProduct denotes sodium/iodide symporter (NIS)
T5 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T6 605-608 DiseaseOrPhenotypicFeature denotes ITD
T7 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T8 668-674 ChemicalEntity denotes iodide
T9 733-739 ChemicalEntity denotes iodide
T10 825-836 ChemicalEntity denotes L-thyroxine
T11 872-883 ChemicalEntity denotes radioiodide
T12 956-977 GeneOrGeneProduct denotes recombinant human TSH
T13 1000-1002 ChemicalEntity denotes I-
T14 1083-1085 ChemicalEntity denotes I-
T15 1162-1170 GeneOrGeneProduct denotes NIS gene
T16 1182-1258 SequenceVariant denotes 15 nucleotide (nt) deletion of the coding sequence (nt 1314 through nt 1328)
T17 1263-1336 SequenceVariant denotes the insertion of 15 nt duplicating the first 15 nt of the adjacent intron
T18 1606-1617 CellLine denotes COS-7 cells
T19 1666-1679 SequenceVariant denotes del-(439-443)
T20 1680-1683 GeneOrGeneProduct denotes NIS
T21 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T22 1911-1919 GeneOrGeneProduct denotes NIS gene

biored-valid-gpt-nr-g

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T3 99-128 DiseaseOrPhenotypicFeature denotes Iodide transport defect (ITD)

biored-valid-gpt-r-g

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 39-47 SequenceVariant denotes deletion
T3 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T4 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T5 124-127 DiseaseOrPhenotypicFeature denotes ITD
T6 208-214 ChemicalEntity denotes iodide
T7 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T8 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T9 496-499 GeneOrGeneProduct denotes NIS
T10 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T11 605-608 DiseaseOrPhenotypicFeature denotes ITD
T12 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T13 668-674 ChemicalEntity denotes iodide
T14 733-739 ChemicalEntity denotes iodide
T15 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism
T16 825-836 ChemicalEntity denotes L-thyroxine
T17 872-883 ChemicalEntity denotes radioiodide
T18 968-973 OrganismTaxon denotes human
T19 974-977 GeneOrGeneProduct denotes TSH
T20 1000-1002 ChemicalEntity denotes I-
T21 1083-1085 ChemicalEntity denotes I-
T22 1162-1170 GeneOrGeneProduct denotes NIS gene
T23 1182-1209 SequenceVariant denotes 15 nucleotide (nt) deletion
T24 1267-1285 SequenceVariant denotes insertion of 15 nt
T25 1374-1392 SequenceVariant denotes insertion/deletion
T26 1452-1460 SequenceVariant denotes deletion
T27 1606-1617 CellLine denotes COS-7 cells
T28 1666-1679 SequenceVariant denotes del-(439-443)
T29 1680-1683 GeneOrGeneProduct denotes NIS
T30 1706-1712 ChemicalEntity denotes iodide
T31 1734-1742 SequenceVariant denotes mutation
T32 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T33 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T34 1895-1903 SequenceVariant denotes deletion
T35 1911-1919 GeneOrGeneProduct denotes NIS gene

biored-valid-gpt-r-ng

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 39-47 SequenceVariant denotes deletion
T3 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T4 99-128 DiseaseOrPhenotypicFeature denotes Iodide transport defect (ITD)
T5 208-214 ChemicalEntity denotes iodide
T6 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T7 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T8 496-499 GeneOrGeneProduct denotes NIS
T9 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T10 605-608 DiseaseOrPhenotypicFeature denotes ITD
T11 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T12 668-674 ChemicalEntity denotes iodide
T13 733-739 ChemicalEntity denotes iodide
T14 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism
T15 825-836 ChemicalEntity denotes L-thyroxine
T16 872-883 ChemicalEntity denotes radioiodide
T17 968-973 OrganismTaxon denotes human
T18 974-977 GeneOrGeneProduct denotes TSH
T19 1000-1002 ChemicalEntity denotes I-
T20 1083-1085 ChemicalEntity denotes I-
T21 1162-1170 GeneOrGeneProduct denotes NIS gene
T22 1182-1209 SequenceVariant denotes 15 nucleotide (nt) deletion
T23 1234-1257 SequenceVariant denotes nt 1314 through nt 1328
T24 1267-1285 SequenceVariant denotes insertion of 15 nt
T25 1286-1313 SequenceVariant denotes duplicating the first 15 nt
T26 1374-1392 SequenceVariant denotes insertion/deletion
T27 1452-1460 SequenceVariant denotes deletion
T28 1606-1617 CellLine denotes COS-7 cells
T29 1666-1679 SequenceVariant denotes del-(439-443)
T30 1680-1683 GeneOrGeneProduct denotes NIS
T31 1706-1712 ChemicalEntity denotes iodide
T32 1734-1742 SequenceVariant denotes mutation
T33 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T34 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T35 1895-1903 SequenceVariant denotes deletion
T36 1911-1919 GeneOrGeneProduct denotes NIS gene

biored-valid-gemini-nr-g

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T3 99-105 ChemicalEntity denotes Iodide
T4 106-128 DiseaseOrPhenotypicFeature denotes transport defect (ITD)
T5 185-192 OrganismTaxon denotes thyroid
T6 208-214 ChemicalEntity denotes iodide
T7 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T8 471-500 GeneOrGeneProduct denotes sodium/iodide symporter (NIS)
T9 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T10 605-608 DiseaseOrPhenotypicFeature denotes ITD
T11 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T12 668-674 ChemicalEntity denotes iodide
T13 689-696 OrganismTaxon denotes thyroid
T14 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism
T15 825-836 ChemicalEntity denotes L-thyroxine
T16 872-883 ChemicalEntity denotes radioiodide
T17 974-977 GeneOrGeneProduct denotes TSH
T18 1054-1061 OrganismTaxon denotes thyroid
T19 1162-1165 GeneOrGeneProduct denotes NIS
T20 1182-1232 SequenceVariant denotes 15 nucleotide (nt) deletion of the coding sequence
T21 1267-1497 SequenceVariant denotes insertion of 15 nt duplicating the first 15 nt of the adjacent intron. The patient was homozygous for this insertion/deletion, while both consanguineous parents were heterozygous. This deletion predicts the production of a protein
T22 1606-1611 CellLine denotes COS-7
T23 1659-1683 GeneOrGeneProduct denotes mutant del-(439-443) NIS
T24 1706-1712 ChemicalEntity denotes iodide
T25 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T26 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism

biored-valid-gpt-r-m

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 39-47 SequenceVariant denotes deletion
T3 55-78 GeneOrGeneProduct denotes sodium/iodide symporter
T4 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T5 124-127 DiseaseOrPhenotypicFeature denotes ITD
T6 208-214 ChemicalEntity denotes iodide
T7 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T8 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T9 496-499 GeneOrGeneProduct denotes NIS
T10 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T11 605-608 DiseaseOrPhenotypicFeature denotes ITD
T12 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T13 668-674 ChemicalEntity denotes iodide
T14 733-739 ChemicalEntity denotes iodide
T15 764-778 DiseaseOrPhenotypicFeature denotes hypothyroidism
T16 825-836 ChemicalEntity denotes L-thyroxine
T17 872-883 ChemicalEntity denotes radioiodide
T18 968-973 OrganismTaxon denotes human
T19 974-977 GeneOrGeneProduct denotes TSH
T20 1000-1002 ChemicalEntity denotes I-
T21 1083-1085 ChemicalEntity denotes I-
T22 1152-1161 OrganismTaxon denotes patient's
T23 1162-1165 GeneOrGeneProduct denotes NIS
T24 1182-1209 SequenceVariant denotes 15 nucleotide (nt) deletion
T25 1267-1285 SequenceVariant denotes insertion of 15 nt
T26 1342-1349 OrganismTaxon denotes patient
T27 1374-1392 SequenceVariant denotes insertion/deletion
T28 1420-1427 OrganismTaxon denotes parents
T29 1452-1460 SequenceVariant denotes deletion
T30 1606-1617 CellLine denotes COS-7 cells
T31 1666-1679 SequenceVariant denotes del-(439-443)
T32 1680-1683 GeneOrGeneProduct denotes NIS
T33 1706-1712 ChemicalEntity denotes iodide
T34 1734-1742 SequenceVariant denotes mutation
T35 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T36 1783-1790 OrganismTaxon denotes patient
T37 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T38 1895-1903 SequenceVariant denotes deletion
T39 1911-1914 GeneOrGeneProduct denotes NIS

biored-valid-gemini-r-m

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 39-47 SequenceVariant denotes deletion
T3 55-86 GeneOrGeneProduct denotes sodium/iodide symporter protein
T4 99-128 DiseaseOrPhenotypicFeature denotes Iodide transport defect (ITD)
T5 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T6 471-500 GeneOrGeneProduct denotes sodium/iodide symporter (NIS)
T7 525-530 OrganismTaxon denotes woman
T8 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T9 605-608 DiseaseOrPhenotypicFeature denotes ITD
T10 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T11 668-674 ChemicalEntity denotes iodide
T12 825-836 ChemicalEntity denotes L-thyroxine
T13 872-883 ChemicalEntity denotes radioiodide
T14 968-973 OrganismTaxon denotes human
T15 974-977 GeneOrGeneProduct denotes TSH
T16 1000-1002 ChemicalEntity denotes I-
T17 1152-1159 OrganismTaxon denotes patient
T18 1162-1170 GeneOrGeneProduct denotes NIS gene
T19 1182-1209 SequenceVariant denotes 15 nucleotide (nt) deletion
T20 1267-1285 SequenceVariant denotes insertion of 15 nt
T21 1374-1392 SequenceVariant denotes insertion/deletion
T22 1420-1427 OrganismTaxon denotes parents
T23 1606-1617 CellLine denotes COS-7 cells
T24 1666-1679 SequenceVariant denotes del-(439-443)
T25 1680-1683 GeneOrGeneProduct denotes NIS
T26 1706-1712 ChemicalEntity denotes iodide
T27 1734-1742 SequenceVariant denotes mutation
T28 1771-1774 DiseaseOrPhenotypicFeature denotes ITD
T29 1783-1790 OrganismTaxon denotes patient
T30 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T31 1895-1903 SequenceVariant denotes deletion
T32 1911-1919 GeneOrGeneProduct denotes NIS gene

biored-valid-deepseek-r-m

Id Subject Object Predicate Lexical cue
T1 0-25 DiseaseOrPhenotypicFeature denotes Congenital hypothyroidism
T2 55-78 GeneOrGeneProduct denotes sodium/iodide symporter
T3 99-122 DiseaseOrPhenotypicFeature denotes Iodide transport defect
T4 124-127 DiseaseOrPhenotypicFeature denotes ITD
T5 307-332 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism
T6 471-494 GeneOrGeneProduct denotes sodium/iodide symporter
T7 496-499 GeneOrGeneProduct denotes NIS
T8 536-550 DiseaseOrPhenotypicFeature denotes hypothyroidism
T9 605-608 DiseaseOrPhenotypicFeature denotes ITD
T10 634-648 DiseaseOrPhenotypicFeature denotes nodular goitre
T11 825-836 ChemicalEntity denotes L-thyroxine
T12 872-883 ChemicalEntity denotes radioiodide
T13 968-973 OrganismTaxon denotes human
T14 974-977 ChemicalEntity denotes TSH
T15 1000-1002 ChemicalEntity denotes I-
T16 1162-1165 GeneOrGeneProduct denotes NIS
T17 1201-1209 SequenceVariant denotes deletion
T18 1267-1276 SequenceVariant denotes insertion
T19 1606-1617 CellLine denotes COS-7 cells
T20 1666-1679 SequenceVariant denotes del-(439-443)
T21 1734-1742 SequenceVariant denotes mutation
T22 1856-1881 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism