PubMed:19353688
Annnotations
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 |