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PubMed:17564961 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 326-334 DiseaseOrPhenotypicFeature denotes cataract 0005129
T2 639-647 DiseaseOrPhenotypicFeature denotes cataract 0005129

DisGeNET

Id Subject Object Predicate Lexical cue
T0 234-238 gene:1421 denotes P23S
T1 303-334 disease:C1832526 denotes polymorphic congenital cataract
T2 222-227 gene:1421 denotes CRYGD
T3 303-334 disease:C1832526 denotes polymorphic congenital cataract
T4 735-740 gene:1421 denotes CRYGD
T5 639-647 disease:C0086543 denotes cataract
R1 T0 T1 associated_with P23S,polymorphic congenital cataract
R2 T2 T3 associated_with CRYGD,polymorphic congenital cataract
R3 T4 T5 associated_with CRYGD,cataract

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 315-334 HP_0000519 denotes congenital cataract
T2 326-334 HP_0000518 denotes cataract
T3 639-647 HP_0000518 denotes cataract
T1 315-334 HP_0000519 denotes congenital cataract
T2 326-334 HP_0000518 denotes cataract
T3 639-647 HP_0000518 denotes cataract

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
17564961-1#44#48#geners28931605 234-238 geners28931605 denotes P23S
17564961-1#113#144#diseaseC1832526 303-334 diseaseC1832526 denotes polymorphic congenital cataract
44#48#geners28931605113#144#diseaseC1832526 17564961-1#44#48#geners28931605 17564961-1#113#144#diseaseC1832526 associated_with P23S,polymorphic congenital cataract

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
17564961-1#32#37#gene1421 222-227 gene1421 denotes CRYGD
17564961-1#44#48#gene1421 234-238 gene1421 denotes P23S
17564961-1#113#144#diseaseC1832526 303-334 diseaseC1832526 denotes polymorphic congenital cataract
17564961-3#100#105#gene1421 735-740 gene1421 denotes CRYGD
17564961-3#4#12#diseaseC0086543 639-647 diseaseC0086543 denotes cataract
32#37#gene1421113#144#diseaseC1832526 17564961-1#32#37#gene1421 17564961-1#113#144#diseaseC1832526 associated_with CRYGD,polymorphic congenital cataract
44#48#gene1421113#144#diseaseC1832526 17564961-1#44#48#gene1421 17564961-1#113#144#diseaseC1832526 associated_with P23S,polymorphic congenital cataract
100#105#gene14214#12#diseaseC0086543 17564961-3#100#105#gene1421 17564961-3#4#12#diseaseC0086543 associated_with CRYGD,cataract