PubMed:11301317 / 0-173
Annnotations
sentences
{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":78},"obj":"Sentence"},{"id":"TextSentencer_T2","span":{"begin":79,"end":150},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":78},"obj":"Sentence"},{"id":"T2","span":{"begin":79,"end":150},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Identification of a dominant negative homeodomain mutation in Rieger syndrome.\nMutations in the PITX2 bicoid-like homeobox gene cause Rieger syndrome. Rieger syndrome is an "}
DisGeNET5_gene_disease
{"project":"DisGeNET5_gene_disease","denotations":[{"id":"11301317-1#17#22#gene5308","span":{"begin":96,"end":101},"obj":"gene5308"},{"id":"11301317-1#35#43#gene10660","span":{"begin":114,"end":122},"obj":"gene10660"},{"id":"11301317-1#55#70#diseaseC0265341","span":{"begin":134,"end":149},"obj":"diseaseC0265341"},{"id":"11301317-1#55#70#diseaseC3495488","span":{"begin":134,"end":149},"obj":"diseaseC3495488"},{"id":"11301317-1#55#70#diseaseC0265341","span":{"begin":134,"end":149},"obj":"diseaseC0265341"},{"id":"11301317-1#55#70#diseaseC3495488","span":{"begin":134,"end":149},"obj":"diseaseC3495488"}],"relations":[{"id":"17#22#gene530855#70#diseaseC0265341","pred":"associated_with","subj":"11301317-1#17#22#gene5308","obj":"11301317-1#55#70#diseaseC0265341"},{"id":"17#22#gene530855#70#diseaseC3495488","pred":"associated_with","subj":"11301317-1#17#22#gene5308","obj":"11301317-1#55#70#diseaseC3495488"},{"id":"17#22#gene530855#70#diseaseC0265341","pred":"associated_with","subj":"11301317-1#17#22#gene5308","obj":"11301317-1#55#70#diseaseC0265341"},{"id":"17#22#gene530855#70#diseaseC3495488","pred":"associated_with","subj":"11301317-1#17#22#gene5308","obj":"11301317-1#55#70#diseaseC3495488"},{"id":"35#43#gene1066055#70#diseaseC0265341","pred":"associated_with","subj":"11301317-1#35#43#gene10660","obj":"11301317-1#55#70#diseaseC0265341"},{"id":"35#43#gene1066055#70#diseaseC3495488","pred":"associated_with","subj":"11301317-1#35#43#gene10660","obj":"11301317-1#55#70#diseaseC3495488"},{"id":"35#43#gene1066055#70#diseaseC0265341","pred":"associated_with","subj":"11301317-1#35#43#gene10660","obj":"11301317-1#55#70#diseaseC0265341"},{"id":"35#43#gene1066055#70#diseaseC3495488","pred":"associated_with","subj":"11301317-1#35#43#gene10660","obj":"11301317-1#55#70#diseaseC3495488"}],"text":"Identification of a dominant negative homeodomain mutation in Rieger syndrome.\nMutations in the PITX2 bicoid-like homeobox gene cause Rieger syndrome. Rieger syndrome is an "}
PubCasesORDO
{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":134,"end":149},"obj":"ORDO:782"},{"id":"TI1","span":{"begin":62,"end":77},"obj":"ORDO:782"},{"id":"AB2","span":{"begin":151,"end":166},"obj":"ORDO:782"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Identification of a dominant negative homeodomain mutation in Rieger syndrome.\nMutations in the PITX2 bicoid-like homeobox gene cause Rieger syndrome. Rieger syndrome is an "}
DisGeNET
{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":114,"end":122},"obj":"gene:10660"},{"id":"T1","span":{"begin":134,"end":149},"obj":"disease:C0265341"},{"id":"T2","span":{"begin":114,"end":122},"obj":"gene:10660"},{"id":"T3","span":{"begin":134,"end":149},"obj":"disease:C3495488"},{"id":"T4","span":{"begin":114,"end":122},"obj":"gene:10660"},{"id":"T5","span":{"begin":134,"end":149},"obj":"disease:C3495489"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"},{"id":"R3","pred":"associated_with","subj":"T4","obj":"T5"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Identification of a dominant negative homeodomain mutation in Rieger syndrome.\nMutations in the PITX2 bicoid-like homeobox gene cause Rieger syndrome. Rieger syndrome is an "}
mondo_disease
{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":62,"end":77},"obj":"Disease"},{"id":"T2","span":{"begin":134,"end":149},"obj":"Disease"},{"id":"T3","span":{"begin":151,"end":166},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0019187"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0019187"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0019187"}],"text":"Identification of a dominant negative homeodomain mutation in Rieger syndrome.\nMutations in the PITX2 bicoid-like homeobox gene cause Rieger syndrome. Rieger syndrome is an "}