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PubMed:22048266 JSONTXT

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TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T1 79-92 DiseaseOrPhenotypicFeature denotes Down syndrome D004314
T2 94-101 DiseaseOrPhenotypicFeature denotes Trisomy D014314
T3 182-195 DiseaseOrPhenotypicFeature denotes Down syndrome D004314
T4 197-199 DiseaseOrPhenotypicFeature denotes DS D004314
T5 341-343 DiseaseOrPhenotypicFeature denotes DS D004314
T6 595-597 DiseaseOrPhenotypicFeature denotes DS D004314
T7 643-645 DiseaseOrPhenotypicFeature denotes DS D004314
T8 862-864 DiseaseOrPhenotypicFeature denotes DS D004314
T9 972-974 DiseaseOrPhenotypicFeature denotes DS D004314
T10 1154-1156 DiseaseOrPhenotypicFeature denotes DS D004314
T11 1347-1349 DiseaseOrPhenotypicFeature denotes DS D004314

TEST-ChemicalEntity

Id Subject Object Predicate Lexical cue ID:
T1 1302-1309 ChemicalEntity denotes leucine http://purl.obolibrary.org/obo/CHEBI_25017
T2 1313-1323 ChemicalEntity denotes methionine http://purl.obolibrary.org/obo/CHEBI_64558|http://purl.obolibrary.org/obo/CHEBI_16811

TEST-OrganismTaxon

Id Subject Object Predicate Lexical cue
T1 464-469 OrganismTaxon denotes virus

Test-SequenceVariant

Id Subject Object Predicate Lexical cue
T1 823-831 SequenceVariant denotes rs461155
T2 919-928 SequenceVariant denotes rs2073601
T3 929-938 SequenceVariant denotes rs2073416
T4 1234-1243 SequenceVariant denotes rs2073601

Test-GeneOrGeneProduct

Id Subject Object Predicate Lexical cue
T1 56-60 GeneOrGeneProduct denotes ETS2
T2 65-69 GeneOrGeneProduct denotes SIM2
T3 414-427 GeneOrGeneProduct denotes Single minded
T4 431-435 GeneOrGeneProduct denotes SIM2
T5 818-822 GeneOrGeneProduct denotes ETS2
T6 899-903 GeneOrGeneProduct denotes SIM2

Test-merged

Id Subject Object Predicate Lexical cue #label ID:
T11 1347-1349 DiseaseOrPhenotypicFeature denotes DS D004314
T10 1154-1156 DiseaseOrPhenotypicFeature denotes DS D004314
T9 972-974 DiseaseOrPhenotypicFeature denotes DS D004314
T8 862-864 DiseaseOrPhenotypicFeature denotes DS D004314
T7 643-645 DiseaseOrPhenotypicFeature denotes DS D004314
T6 595-597 DiseaseOrPhenotypicFeature denotes DS D004314
T5 341-343 DiseaseOrPhenotypicFeature denotes DS D004314
T4 197-199 DiseaseOrPhenotypicFeature denotes DS D004314
T3 182-195 DiseaseOrPhenotypicFeature denotes Down syndrome D004314
T2 94-101 DiseaseOrPhenotypicFeature denotes Trisomy D014314
T1 79-92 DiseaseOrPhenotypicFeature denotes Down syndrome D004314
T47519 464-469 OrganismTaxon denotes virus
T7832 899-903 GeneOrGeneProduct denotes SIM2
T50635 818-822 GeneOrGeneProduct denotes ETS2
T66568 431-435 GeneOrGeneProduct denotes SIM2
T4116 414-427 GeneOrGeneProduct denotes Single minded
T73982 65-69 GeneOrGeneProduct denotes SIM2
T19259 56-60 GeneOrGeneProduct denotes ETS2
T21327 1313-1323 ChemicalEntity denotes methionine http://purl.obolibrary.org/obo/CHEBI_16811|http://purl.obolibrary.org/obo/CHEBI_64558
T5347 1302-1309 ChemicalEntity denotes leucine http://purl.obolibrary.org/obo/CHEBI_25017
T75054 1234-1243 SequenceVariant denotes rs2073601
T5052 929-938 SequenceVariant denotes rs2073416
T10725 919-928 SequenceVariant denotes rs2073601
T71771 823-831 SequenceVariant denotes rs461155

Test-merged-2

Id Subject Object Predicate Lexical cue #label ID:
T71771 823-831 SequenceVariant denotes rs461155
T10725 919-928 SequenceVariant denotes rs2073601
T5052 929-938 SequenceVariant denotes rs2073416
T75054 1234-1243 SequenceVariant denotes rs2073601
T5347 1302-1309 ChemicalEntity denotes leucine http://purl.obolibrary.org/obo/CHEBI_25017
T21327 1313-1323 ChemicalEntity denotes methionine http://purl.obolibrary.org/obo/CHEBI_64558|http://purl.obolibrary.org/obo/CHEBI_16811
T19259 56-60 GeneOrGeneProduct denotes ETS2
T73982 65-69 GeneOrGeneProduct denotes SIM2
T4116 414-427 GeneOrGeneProduct denotes Single minded
T66568 431-435 GeneOrGeneProduct denotes SIM2
T50635 818-822 GeneOrGeneProduct denotes ETS2
T7832 899-903 GeneOrGeneProduct denotes SIM2
T47519 464-469 OrganismTaxon denotes virus
T1 79-92 DiseaseOrPhenotypicFeature denotes Down syndrome D004314
T2 94-101 DiseaseOrPhenotypicFeature denotes Trisomy D014314
T3 182-195 DiseaseOrPhenotypicFeature denotes Down syndrome D004314
T4 197-199 DiseaseOrPhenotypicFeature denotes DS D004314
T5 341-343 DiseaseOrPhenotypicFeature denotes DS D004314
T6 595-597 DiseaseOrPhenotypicFeature denotes DS D004314
T7 643-645 DiseaseOrPhenotypicFeature denotes DS D004314
T8 862-864 DiseaseOrPhenotypicFeature denotes DS D004314
T9 972-974 DiseaseOrPhenotypicFeature denotes DS D004314
T10 1154-1156 DiseaseOrPhenotypicFeature denotes DS D004314
T11 1347-1349 DiseaseOrPhenotypicFeature denotes DS D004314

DisGeNET

Id Subject Object Predicate Lexical cue
T0 65-69 gene:6493 denotes SIM2
T1 79-92 disease:C0013080 denotes Down syndrome
T2 56-60 gene:2114 denotes ETS2
T3 79-92 disease:C0013080 denotes Down syndrome
T4 431-435 gene:6493 denotes SIM2
T5 447-463 disease:C0272138 denotes erythroblastosis
T6 431-435 gene:6493 denotes SIM2
T7 595-597 disease:C0013080 denotes DS
T8 818-822 gene:2114 denotes ETS2
T9 862-864 disease:C0013080 denotes DS
T10 899-903 gene:6493 denotes SIM2
T11 972-974 disease:C0013080 denotes DS
R1 T0 T1 associated_with SIM2,Down syndrome
R2 T2 T3 associated_with ETS2,Down syndrome
R3 T4 T5 associated_with SIM2,erythroblastosis
R4 T6 T7 associated_with SIM2,DS
R5 T8 T9 associated_with ETS2,DS
R6 T10 T11 associated_with SIM2,DS

Allie

Id Subject Object Predicate Lexical cue
SS1_22048266_1_0 182-195 expanded denotes Down syndrome
SS2_22048266_1_0 197-199 abbr denotes DS
SS1_22048266_3_0 414-429 expanded denotes Single minded 2
SS2_22048266_3_0 431-435 abbr denotes SIM2
AE1_22048266_1_0 SS1_22048266_1_0 SS2_22048266_1_0 abbreviatedTo Down syndrome,DS
AE1_22048266_3_0 SS1_22048266_3_0 SS2_22048266_3_0 abbreviatedTo Single minded 2,SIM2

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 823-831 SNP:rs461155 denotes rs461155
T2 919-928 SNP:rs2073601 denotes rs2073601
T3 929-938 SNP:rs2073416 denotes rs2073416
T4 1234-1243 SNP:rs2073601 denotes rs2073601