Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
T1 |
35-39 |
DiseaseOrPhenotypicFeature |
denotes |
MKS3 |
0011821 |
T2 |
54-70 |
DiseaseOrPhenotypicFeature |
denotes |
nephronophthisis |
0019005 |
T3 |
92-98 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP11 |
0013302 |
T4 |
113-129 |
DiseaseOrPhenotypicFeature |
denotes |
Nephronophthisis |
0019005 |
T5 |
131-135 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP |
0019005 |
T6 |
155-176 |
DiseaseOrPhenotypicFeature |
denotes |
cystic kidney disease |
0002473 |
T7 |
216-237 |
DiseaseOrPhenotypicFeature |
denotes |
chronic renal failure |
0024327 |
T8 |
293-300 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP1-9 |
0014537 |
T9 |
324-328 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP |
0019005 |
T10 |
329-332 |
DiseaseOrPhenotypicFeature |
denotes |
can |
0012833 |
T11 |
352-372 |
DiseaseOrPhenotypicFeature |
denotes |
retinal degeneration |
0004580 |
T12 |
374-395 |
DiseaseOrPhenotypicFeature |
denotes |
Senior-Løken syndrome |
0017842|0009962 |
T14 |
434-450 |
DiseaseOrPhenotypicFeature |
denotes |
Joubert syndrome |
0018772|0008944 |
T16 |
915-919 |
DiseaseOrPhenotypicFeature |
denotes |
MKS3 |
0011821 |
T17 |
994-998 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP |
0019005 |
T18 |
1146-1150 |
DiseaseOrPhenotypicFeature |
denotes |
MKS3 |
0011821 |
T19 |
1177-1199 |
DiseaseOrPhenotypicFeature |
denotes |
Meckel-Gruber syndrome |
0018921|0009571 |
T21 |
1201-1204 |
DiseaseOrPhenotypicFeature |
denotes |
MKS |
0009571|0018921 |
T23 |
1217-1233 |
DiseaseOrPhenotypicFeature |
denotes |
Joubert syndrome |
0018772|0008944 |
T25 |
1235-1239 |
DiseaseOrPhenotypicFeature |
denotes |
JBTS |
0018772 |
T26 |
1347-1351 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP |
0019005 |
T27 |
1537-1540 |
DiseaseOrPhenotypicFeature |
denotes |
MKS |
0009571|0018921 |
T29 |
1544-1548 |
DiseaseOrPhenotypicFeature |
denotes |
JBTS |
0018772 |
T30 |
1596-1600 |
DiseaseOrPhenotypicFeature |
denotes |
MKS3 |
0011821 |
T31 |
1629-1633 |
DiseaseOrPhenotypicFeature |
denotes |
JBTS |
0018772 |
T32 |
1784-1788 |
DiseaseOrPhenotypicFeature |
denotes |
MKS3 |
0011821 |
T33 |
1812-1816 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP |
0019005 |
T34 |
1838-1844 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP11 |
0013302 |
T35 |
1875-1879 |
DiseaseOrPhenotypicFeature |
denotes |
MKS3 |
0011821 |
T36 |
1964-1968 |
DiseaseOrPhenotypicFeature |
denotes |
NPHP |
0019005 |
T37 |
1970-1974 |
DiseaseOrPhenotypicFeature |
denotes |
JBTS |
0018772 |
T38 |
1980-1983 |
DiseaseOrPhenotypicFeature |
denotes |
MKS |
0009571|0018921 |