| Id |
Subject |
Object |
Predicate |
Lexical cue |
db_id |
| 2466 |
17-22 |
SequenceVariant |
denotes |
M404V |
DBSNP:rs771966860 |
| 2467 |
39-42 |
GeneOrGeneProduct |
denotes |
p62 |
NCBIGene:8878 |
| 2468 |
43-57 |
GeneOrGeneProduct |
denotes |
sequestosome 1 |
NCBIGene:8878 |
| 2469 |
59-62 |
GeneOrGeneProduct |
denotes |
p62 |
NCBIGene:8878 |
| 2470 |
63-69 |
GeneOrGeneProduct |
denotes |
SQSTM1 |
NCBIGene:8878 |
| 2471 |
93-116 |
DiseaseOrPhenotypicFeature |
denotes |
Paget's disease of bone |
MESH:C538098 |
| 2472 |
156-159 |
GeneOrGeneProduct |
denotes |
p62 |
NCBIGene:8878 |
| 2473 |
160-174 |
GeneOrGeneProduct |
denotes |
Sequestosome 1 |
NCBIGene:8878 |
| 2474 |
181-184 |
GeneOrGeneProduct |
denotes |
p62 |
NCBIGene:8878 |
| 2475 |
185-191 |
GeneOrGeneProduct |
denotes |
SQSTM1 |
NCBIGene:8878 |
| 2476 |
241-264 |
DiseaseOrPhenotypicFeature |
denotes |
Paget's disease of bone |
MESH:C538098 |
| 2477 |
266-269 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |
| 2478 |
298-343 |
SequenceVariant |
denotes |
methionine-->valine substitution at codon 404 |
DBSNP:rs771966860 |
| 2479 |
345-350 |
SequenceVariant |
denotes |
M404V |
DBSNP:rs771966860 |
| 2480 |
406-409 |
GeneOrGeneProduct |
denotes |
p62 |
NCBIGene:8878 |
| 2481 |
410-416 |
GeneOrGeneProduct |
denotes |
SQSTM1 |
NCBIGene:8878 |
| 2482 |
436-439 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |
| 2483 |
440-447 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 2484 |
481-488 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 2485 |
541-544 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |
| 2486 |
646-651 |
SequenceVariant |
denotes |
M404V |
DBSNP:rs771966860 |
| 2487 |
682-685 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |
| 2488 |
854-857 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |
| 2489 |
858-866 |
OrganismTaxon |
denotes |
patients |
NCBITaxon:9606 |
| 2490 |
991-996 |
SequenceVariant |
denotes |
M404V |
DBSNP:rs771966860 |
| 2491 |
1044-1047 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |
| 2492 |
1060-1067 |
OrganismTaxon |
denotes |
patient |
NCBITaxon:9606 |
| 2493 |
1134-1153 |
DiseaseOrPhenotypicFeature |
denotes |
polyostotic disease |
MESH:D005357 |
| 2494 |
1317-1322 |
SequenceVariant |
denotes |
M404V |
DBSNP:rs771966860 |
| 2495 |
1411-1431 |
ChemicalEntity |
denotes |
alkaline phosphatase |
MESH:D000469 |
| 2496 |
1572-1577 |
SequenceVariant |
denotes |
M404V |
DBSNP:rs771966860 |
| 2497 |
1594-1597 |
GeneOrGeneProduct |
denotes |
p62 |
NCBIGene:8878 |
| 2498 |
1598-1604 |
GeneOrGeneProduct |
denotes |
SQSTM1 |
NCBIGene:8878 |
| 2499 |
1636-1639 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |
| 2500 |
1683-1686 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |
| 2501 |
1899-1902 |
GeneOrGeneProduct |
denotes |
p62 |
NCBIGene:8878 |
| 2502 |
1903-1909 |
GeneOrGeneProduct |
denotes |
SQSTM1 |
NCBIGene:8878 |
| 2503 |
1963-1966 |
DiseaseOrPhenotypicFeature |
denotes |
PDB |
MESH:C538098 |