| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
ID: |
| T6891 |
26-33 |
ChemicalEntity |
denotes |
calcium |
|
D002118|http://purl.obolibrary.org/obo/CHEBI_29320|http://purl.obolibrary.org/obo/CHEBI_22984 |
| T14074 |
26-41 |
GeneOrGeneProduct |
denotes |
calcium-channel |
|
|
| T39385 |
50-58 |
GeneOrGeneProduct |
denotes |
CACNA2D4 |
|
|
| T1 |
86-100 |
DiseaseOrPhenotypicFeature |
denotes |
cone dystrophy |
D000077765 |
|
| T10600 |
102-109 |
ChemicalEntity |
denotes |
Retinal |
|
http://purl.obolibrary.org/obo/CHEBI_17898 |
| T26626 |
183-190 |
ChemicalEntity |
denotes |
calcium |
|
D002118|http://purl.obolibrary.org/obo/CHEBI_29320|http://purl.obolibrary.org/obo/CHEBI_22984 |
| T43972 |
183-199 |
GeneOrGeneProduct |
denotes |
calcium channels |
|
|
| T38311 |
217-223 |
GeneOrGeneProduct |
denotes |
ribbon |
|
|
| T43413 |
297-305 |
GeneOrGeneProduct |
denotes |
Cacna2d4 |
|
|
| T79427 |
328-333 |
OrganismTaxon |
denotes |
mouse |
|
|
| T36328 |
363-370 |
ChemicalEntity |
denotes |
retinal |
|
D012172|http://purl.obolibrary.org/obo/CHEBI_15035 |
| T80950 |
411-417 |
GeneOrGeneProduct |
denotes |
ribbon |
|
|
| T7 |
450-458 |
GeneOrGeneProduct |
denotes |
Cacna2d4 |
|
|
| T24001 |
482-489 |
ChemicalEntity |
denotes |
calcium |
|
D002118|http://purl.obolibrary.org/obo/CHEBI_29320|http://purl.obolibrary.org/obo/CHEBI_22984 |
| T8 |
482-497 |
GeneOrGeneProduct |
denotes |
calcium-channel |
|
|
| T9 |
523-528 |
GeneOrGeneProduct |
denotes |
alpha |
|
|
| T75998 |
533-538 |
OrganismTaxon |
denotes |
delta |
|
|
| T20409 |
562-567 |
OrganismTaxon |
denotes |
human |
|
|
| T10 |
580-588 |
GeneOrGeneProduct |
denotes |
CACNA2D4 |
|
|
| T13510 |
679-687 |
OrganismTaxon |
denotes |
patients |
|
|
| T2 |
725-740 |
DiseaseOrPhenotypicFeature |
denotes |
night blindness |
D009755 |
|
| T84447 |
825-830 |
SequenceVariant |
denotes |
2406C |
|
|
| T11 |
839-847 |
GeneOrGeneProduct |
denotes |
CACNA2D4 |
|
|
| T5 |
967-975 |
OrganismTaxon |
denotes |
patients |
|
|
| T3 |
1013-1027 |
DiseaseOrPhenotypicFeature |
denotes |
cone dystrophy |
D000077765 |
|
| T6 |
1092-1097 |
OrganismTaxon |
denotes |
human |
|
|
| T12 |
1098-1106 |
GeneOrGeneProduct |
denotes |
CACNA2D4 |
|
|
| T13 |
1125-1135 |
GeneOrGeneProduct |
denotes |
novel gene |
|
|
| T4 |
1175-1189 |
DiseaseOrPhenotypicFeature |
denotes |
cone dystrophy |
D000077765 |
|
