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PubMed:7811247 / 0-201 JSONTXT

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TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T1 9-29 DiseaseOrPhenotypicFeature denotes adrenoleukodystrophy D000326
T2 31-34 DiseaseOrPhenotypicFeature denotes ALD D000326
T3 61-64 DiseaseOrPhenotypicFeature denotes ALD D000326
T4 152-172 DiseaseOrPhenotypicFeature denotes adrenoleukodystrophy D000326
T5 174-177 DiseaseOrPhenotypicFeature denotes ALD D000326

TEST-OrganismTaxon

Id Subject Object Predicate Lexical cue
T1 191-198 OrganismTaxon denotes patient

Test-merged

Id Subject Object Predicate Lexical cue #label
T5 174-177 DiseaseOrPhenotypicFeature denotes ALD D000326
T4 152-172 DiseaseOrPhenotypicFeature denotes adrenoleukodystrophy D000326
T3 61-64 DiseaseOrPhenotypicFeature denotes ALD D000326
T2 31-34 DiseaseOrPhenotypicFeature denotes ALD D000326
T1 9-29 DiseaseOrPhenotypicFeature denotes adrenoleukodystrophy D000326
T45995 191-198 OrganismTaxon denotes patient

Test-merged-2

Id Subject Object Predicate Lexical cue #label
T45995 191-198 OrganismTaxon denotes patient
T1 9-29 DiseaseOrPhenotypicFeature denotes adrenoleukodystrophy D000326
T2 31-34 DiseaseOrPhenotypicFeature denotes ALD D000326
T3 61-64 DiseaseOrPhenotypicFeature denotes ALD D000326
T4 152-172 DiseaseOrPhenotypicFeature denotes adrenoleukodystrophy D000326
T5 174-177 DiseaseOrPhenotypicFeature denotes ALD D000326

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-134 Sentence denotes X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes.
T1 0-134 Sentence denotes X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes.

DisGeNET

Id Subject Object Predicate Lexical cue
T0 61-64 gene:215 denotes ALD
T1 0-29 disease:C0162309 denotes X-linked adrenoleukodystrophy
T2 61-64 gene:215 denotes ALD
T3 31-34 disease:C0162309 denotes ALD
R1 T0 T1 associated_with ALD,X-linked adrenoleukodystrophy
R2 T2 T3 associated_with ALD,ALD

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
7811247-0#61#64#gene215 61-64 gene215 denotes ALD
7811247-0#0#29#diseaseC0162309 0-29 diseaseC0162309 denotes X-linked adrenoleukodystrophy
7811247-0#31#34#diseaseC0162309 31-34 diseaseC0162309 denotes ALD
61#64#gene2150#29#diseaseC0162309 7811247-0#61#64#gene215 7811247-0#0#29#diseaseC0162309 associated_with ALD,X-linked adrenoleukodystrophy
61#64#gene21531#34#diseaseC0162309 7811247-0#61#64#gene215 7811247-0#31#34#diseaseC0162309 associated_with ALD,ALD

PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 0-29 ORDO:43 denotes X-linked adrenoleukodystrophy
TI2 31-34 ORDO:43 denotes ALD
AB1 174-177 ORDO:43 denotes ALD
TI3 61-64 ORDO:43 denotes ALD

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 0-29 SpecificDisease:D000326 denotes X-linked adrenoleukodystrophy
T2 31-34 SpecificDisease:D000326 denotes ALD
T3 61-64 Modifier:D000326 denotes ALD
T4 152-172 Modifier:D000326 denotes adrenoleukodystrophy
T5 174-177 Modifier:D000326 denotes ALD