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PubMed:11301317 / 0-198 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-78 Sentence denotes Identification of a dominant negative homeodomain mutation in Rieger syndrome.
TextSentencer_T2 79-150 Sentence denotes Mutations in the PITX2 bicoid-like homeobox gene cause Rieger syndrome.
T1 0-78 Sentence denotes Identification of a dominant negative homeodomain mutation in Rieger syndrome.
T2 79-150 Sentence denotes Mutations in the PITX2 bicoid-like homeobox gene cause Rieger syndrome.

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
11301317-1#17#22#gene5308 96-101 gene5308 denotes PITX2
11301317-1#35#43#gene10660 114-122 gene10660 denotes homeobox
11301317-1#55#70#diseaseC0265341 134-149 diseaseC0265341 denotes Rieger syndrome
11301317-1#55#70#diseaseC3495488 134-149 diseaseC3495488 denotes Rieger syndrome
11301317-1#55#70#diseaseC0265341 134-149 diseaseC0265341 denotes Rieger syndrome
11301317-1#55#70#diseaseC3495488 134-149 diseaseC3495488 denotes Rieger syndrome
17#22#gene530855#70#diseaseC0265341 11301317-1#17#22#gene5308 11301317-1#55#70#diseaseC0265341 associated_with PITX2,Rieger syndrome
17#22#gene530855#70#diseaseC3495488 11301317-1#17#22#gene5308 11301317-1#55#70#diseaseC3495488 associated_with PITX2,Rieger syndrome
17#22#gene530855#70#diseaseC0265341 11301317-1#17#22#gene5308 11301317-1#55#70#diseaseC0265341 associated_with PITX2,Rieger syndrome
17#22#gene530855#70#diseaseC3495488 11301317-1#17#22#gene5308 11301317-1#55#70#diseaseC3495488 associated_with PITX2,Rieger syndrome
35#43#gene1066055#70#diseaseC0265341 11301317-1#35#43#gene10660 11301317-1#55#70#diseaseC0265341 associated_with homeobox,Rieger syndrome
35#43#gene1066055#70#diseaseC3495488 11301317-1#35#43#gene10660 11301317-1#55#70#diseaseC3495488 associated_with homeobox,Rieger syndrome
35#43#gene1066055#70#diseaseC0265341 11301317-1#35#43#gene10660 11301317-1#55#70#diseaseC0265341 associated_with homeobox,Rieger syndrome
35#43#gene1066055#70#diseaseC3495488 11301317-1#35#43#gene10660 11301317-1#55#70#diseaseC3495488 associated_with homeobox,Rieger syndrome

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 134-149 ORDO:782 denotes Rieger syndrome
TI1 62-77 ORDO:782 denotes Rieger syndrome
AB2 151-166 ORDO:782 denotes Rieger syndrome

DisGeNET

Id Subject Object Predicate Lexical cue
T0 114-122 gene:10660 denotes homeobox
T1 134-149 disease:C0265341 denotes Rieger syndrome
T2 114-122 gene:10660 denotes homeobox
T3 134-149 disease:C3495488 denotes Rieger syndrome
T4 114-122 gene:10660 denotes homeobox
T5 134-149 disease:C3495489 denotes Rieger syndrome
R1 T0 T1 associated_with homeobox,Rieger syndrome
R2 T2 T3 associated_with homeobox,Rieger syndrome
R3 T4 T5 associated_with homeobox,Rieger syndrome

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 62-77 Disease denotes Rieger syndrome http://purl.obolibrary.org/obo/MONDO_0019187
T2 134-149 Disease denotes Rieger syndrome http://purl.obolibrary.org/obo/MONDO_0019187
T3 151-166 Disease denotes Rieger syndrome http://purl.obolibrary.org/obo/MONDO_0019187

NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T1 192-197 OrganismTaxon denotes human 9606