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PubMed:19353688 JSONTXT

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TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T1 5-13 DiseaseOrPhenotypicFeature denotes monosomy D009006
T2 23-30 DiseaseOrPhenotypicFeature denotes trisomy D014314
T3 165-184 DiseaseOrPhenotypicFeature denotes auditory neuropathy C538268
T4 333-348 DiseaseOrPhenotypicFeature denotes partial trisomy D014314
T5 352-360 DiseaseOrPhenotypicFeature denotes monosomy D009006
T6 698-706 DiseaseOrPhenotypicFeature denotes monosomy D009006
T7 716-724 DiseaseOrPhenotypicFeature denotes deafness D003638
T8 726-743 DiseaseOrPhenotypicFeature denotes duodenal stenosis C535720
T9 763-775 DiseaseOrPhenotypicFeature denotes growth delay DISEASE
T10 827-834 DiseaseOrPhenotypicFeature denotes trisomy D014314
T11 891-899 DiseaseOrPhenotypicFeature denotes deafness D003638
T12 1025-1033 DiseaseOrPhenotypicFeature denotes deafness D003638
T13 1366-1374 DiseaseOrPhenotypicFeature denotes deafness D003638
T14 1413-1421 DiseaseOrPhenotypicFeature denotes deafness D003638
T15 1438-1446 DiseaseOrPhenotypicFeature denotes monosomy D009006
T16 1462-1470 DiseaseOrPhenotypicFeature denotes deafness D003638
T17 1487-1495 DiseaseOrPhenotypicFeature denotes monosomy D009006

TEST-OrganismTaxon

Id Subject Object Predicate Lexical cue
T1 777-786 OrganismTaxon denotes vertebral
T2 1312-1319 OrganismTaxon denotes patient

Test-merged

Id Subject Object Predicate Lexical cue #label
T17 1487-1495 DiseaseOrPhenotypicFeature denotes monosomy D009006
T16 1462-1470 DiseaseOrPhenotypicFeature denotes deafness D003638
T15 1438-1446 DiseaseOrPhenotypicFeature denotes monosomy D009006
T14 1413-1421 DiseaseOrPhenotypicFeature denotes deafness D003638
T13 1366-1374 DiseaseOrPhenotypicFeature denotes deafness D003638
T12 1025-1033 DiseaseOrPhenotypicFeature denotes deafness D003638
T11 891-899 DiseaseOrPhenotypicFeature denotes deafness D003638
T10 827-834 DiseaseOrPhenotypicFeature denotes trisomy D014314
T9 763-775 DiseaseOrPhenotypicFeature denotes growth delay DISEASE
T8 726-743 DiseaseOrPhenotypicFeature denotes duodenal stenosis C535720
T7 716-724 DiseaseOrPhenotypicFeature denotes deafness D003638
T6 698-706 DiseaseOrPhenotypicFeature denotes monosomy D009006
T5 352-360 DiseaseOrPhenotypicFeature denotes monosomy D009006
T4 333-348 DiseaseOrPhenotypicFeature denotes partial trisomy D014314
T3 165-184 DiseaseOrPhenotypicFeature denotes auditory neuropathy C538268
T2 23-30 DiseaseOrPhenotypicFeature denotes trisomy D014314
T1 5-13 DiseaseOrPhenotypicFeature denotes monosomy D009006
T47837 1312-1319 OrganismTaxon denotes patient
T75283 777-786 OrganismTaxon denotes vertebral
T50253 1776-1781 GeneOrGeneProduct denotes extra
T38572 1360-1365 GeneOrGeneProduct denotes AUNA1
T48581 1265-1273 GeneOrGeneProduct denotes retained
T97445 1241-1246 GeneOrGeneProduct denotes AUNA1
T73161 1151-1156 GeneOrGeneProduct denotes PCDH9
T90556 1119-1124 GeneOrGeneProduct denotes AUNA1
T2215 978-983 GeneOrGeneProduct denotes PCDH9
T16597 948-963 GeneOrGeneProduct denotes protocadherin-9
T72188 941-946 GeneOrGeneProduct denotes PCDH9
T8306 885-890 GeneOrGeneProduct denotes AUNA1
T1153 186-191 GeneOrGeneProduct denotes AUNA1
T84697 112-117 GeneOrGeneProduct denotes PCDH9

Test-GeneOrGeneProduct

Id Subject Object Predicate Lexical cue
T1 112-117 GeneOrGeneProduct denotes PCDH9
T2 186-191 GeneOrGeneProduct denotes AUNA1
T3 735-743 GeneOrGeneProduct denotes stenosis
T4 885-890 GeneOrGeneProduct denotes AUNA1
T5 941-946 GeneOrGeneProduct denotes PCDH9
T6 948-963 GeneOrGeneProduct denotes protocadherin-9
T7 978-983 GeneOrGeneProduct denotes PCDH9
T8 1119-1124 GeneOrGeneProduct denotes AUNA1
T9 1151-1156 GeneOrGeneProduct denotes PCDH9
T10 1241-1246 GeneOrGeneProduct denotes AUNA1
T11 1265-1273 GeneOrGeneProduct denotes retained
T12 1360-1365 GeneOrGeneProduct denotes AUNA1
T13 1776-1781 GeneOrGeneProduct denotes extra

Test-merged-2

Id Subject Object Predicate Lexical cue #label
T84697 112-117 GeneOrGeneProduct denotes PCDH9
T1153 186-191 GeneOrGeneProduct denotes AUNA1
T23323 735-743 GeneOrGeneProduct denotes stenosis
T8306 885-890 GeneOrGeneProduct denotes AUNA1
T72188 941-946 GeneOrGeneProduct denotes PCDH9
T16597 948-963 GeneOrGeneProduct denotes protocadherin-9
T2215 978-983 GeneOrGeneProduct denotes PCDH9
T90556 1119-1124 GeneOrGeneProduct denotes AUNA1
T73161 1151-1156 GeneOrGeneProduct denotes PCDH9
T97445 1241-1246 GeneOrGeneProduct denotes AUNA1
T48581 1265-1273 GeneOrGeneProduct denotes retained
T38572 1360-1365 GeneOrGeneProduct denotes AUNA1
T50253 1776-1781 GeneOrGeneProduct denotes extra
T75283 777-786 OrganismTaxon denotes vertebral
T47837 1312-1319 OrganismTaxon denotes patient
T1 5-13 DiseaseOrPhenotypicFeature denotes monosomy D009006
T2 23-30 DiseaseOrPhenotypicFeature denotes trisomy D014314
T3 165-184 DiseaseOrPhenotypicFeature denotes auditory neuropathy C538268
T4 333-348 DiseaseOrPhenotypicFeature denotes partial trisomy D014314
T5 352-360 DiseaseOrPhenotypicFeature denotes monosomy D009006
T6 698-706 DiseaseOrPhenotypicFeature denotes monosomy D009006
T7 716-724 DiseaseOrPhenotypicFeature denotes deafness D003638
T8 726-743 DiseaseOrPhenotypicFeature denotes duodenal stenosis C535720
T9 763-775 DiseaseOrPhenotypicFeature denotes growth delay DISEASE
T10 827-834 DiseaseOrPhenotypicFeature denotes trisomy D014314
T11 891-899 DiseaseOrPhenotypicFeature denotes deafness D003638
T12 1025-1033 DiseaseOrPhenotypicFeature denotes deafness D003638
T13 1366-1374 DiseaseOrPhenotypicFeature denotes deafness D003638
T14 1413-1421 DiseaseOrPhenotypicFeature denotes deafness D003638
T15 1438-1446 DiseaseOrPhenotypicFeature denotes monosomy D009006
T16 1462-1470 DiseaseOrPhenotypicFeature denotes deafness D003638
T17 1487-1495 DiseaseOrPhenotypicFeature denotes monosomy D009006

DisGeNET

Id Subject Object Predicate Lexical cue
T0 112-117 gene:5101 denotes PCDH9
T1 23-30 disease:C0041107 denotes trisomy
T2 112-117 gene:5101 denotes PCDH9
T3 165-184 disease:C1852271 denotes auditory neuropathy
T4 112-117 gene:5101 denotes PCDH9
T5 186-191 disease:C1852271 denotes AUNA1
T6 948-963 gene:5101 denotes protocadherin-9
T7 885-890 disease:C1852271 denotes AUNA1
T8 1151-1156 gene:5101 denotes PCDH9
T9 1119-1124 disease:C1852271 denotes AUNA1
R1 T0 T1 associated_with PCDH9,trisomy
R2 T2 T3 associated_with PCDH9,auditory neuropathy
R3 T4 T5 associated_with PCDH9,AUNA1
R4 T6 T7 associated_with protocadherin-9,AUNA1
R5 T8 T9 associated_with PCDH9,AUNA1

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 726-743 HP:0100867 denotes duodenal stenosis
AB2 763-775 HP:0001510 denotes growth delay