| Id |
Subject |
Object |
Predicate |
Lexical cue |
#label |
ID: |
| T21286 |
16-47 |
GeneOrGeneProduct |
denotes |
inducible nitric oxide synthase |
|
|
| T1 |
26-47 |
ChemicalEntity |
denotes |
nitric oxide synthase |
|
D019001 |
| T43926 |
62-70 |
DiseaseOrPhenotypicFeature |
denotes |
glaucoma |
D005901 |
|
| T74811 |
101-115 |
GeneOrGeneProduct |
denotes |
nuclear factor |
|
|
| T2 |
134-146 |
ChemicalEntity |
denotes |
Nitric oxide |
|
http://purl.obolibrary.org/obo/CHEBI_16480 |
| T19901 |
184-189 |
OrganismTaxon |
denotes |
human |
|
|
| T27754 |
346-389 |
DiseaseOrPhenotypicFeature |
denotes |
neurological and non-neurological disorders |
DISEASE |
|
| T3 |
475-496 |
ChemicalEntity |
denotes |
Nitric Oxide Synthase |
|
D019001 |
| T31184 |
475-496 |
GeneOrGeneProduct |
denotes |
Nitric Oxide Synthase |
|
|
| T4 |
498-502 |
GeneOrGeneProduct |
denotes |
iNOS |
|
|
| T50349 |
512-547 |
DiseaseOrPhenotypicFeature |
denotes |
neuropathological disorder glaucoma |
DISEASE |
|
| T74053 |
576-585 |
DiseaseOrPhenotypicFeature |
denotes |
blindness |
D001766 |
|
| T5 |
670-674 |
GeneOrGeneProduct |
denotes |
iNOS |
|
|
| T88947 |
679-706 |
DiseaseOrPhenotypicFeature |
denotes |
primary open angle glaucoma |
D005902 |
|
| T73675 |
708-712 |
DiseaseOrPhenotypicFeature |
denotes |
POAG |
DISEASE |
|
| T6 |
925-929 |
GeneOrGeneProduct |
denotes |
iNOS |
|
|
| T6481 |
952-956 |
DiseaseOrPhenotypicFeature |
denotes |
POAG |
DISEASE |
|
| T56191 |
957-965 |
OrganismTaxon |
denotes |
patients |
|
|
| T7 |
1048-1063 |
GeneOrGeneProduct |
denotes |
protein-binding |
|
|
| T8 |
1064-1074 |
GeneOrGeneProduct |
denotes |
capability |
|
|
| T21509 |
1229-1237 |
OrganismTaxon |
denotes |
patients |
|
|
| T26403 |
1373-1377 |
DiseaseOrPhenotypicFeature |
denotes |
POAG |
DISEASE |
|
| T4112 |
1378-1386 |
OrganismTaxon |
denotes |
patients |
|
|
| T9 |
1496-1512 |
GeneOrGeneProduct |
denotes |
nuclear proteins |
|
|
| T38418 |
1638-1645 |
OrganismTaxon |
denotes |
time, a |
|
|
| T10 |
1669-1673 |
GeneOrGeneProduct |
denotes |
iNOS |
|
|
| T99485 |
1679-1683 |
DiseaseOrPhenotypicFeature |
denotes |
POAG |
DISEASE |
|
