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PubMed:19546241 JSONTXT

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DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
19546241-2#156#194#gene545 477-515 gene545 denotes ataxia telangiectasia and Rad3 related
19546241-2#196#199#gene545 517-520 gene545 denotes ATR
19546241-2#217#221#gene5116 538-542 gene5116 denotes PCNT
19546241-2#108#123#diseaseC0265202 429-444 diseaseC0265202 denotes Seckel syndrome
156#194#gene545108#123#diseaseC0265202 19546241-2#156#194#gene545 19546241-2#108#123#diseaseC0265202 associated_with ataxia telangiectasia and Rad3 related,Seckel syndrome
196#199#gene545108#123#diseaseC0265202 19546241-2#196#199#gene545 19546241-2#108#123#diseaseC0265202 associated_with ATR,Seckel syndrome
217#221#gene5116108#123#diseaseC0265202 19546241-2#217#221#gene5116 19546241-2#108#123#diseaseC0265202 associated_with PCNT,Seckel syndrome

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 85-105 DiseaseOrPhenotypicFeature denotes Primary microcephaly 0016056
T2 107-122 DiseaseOrPhenotypicFeature denotes Seckel syndrome 0019342
T3 128-185 DiseaseOrPhenotypicFeature denotes microcephalic osteodysplastic primordial dwarfism type II 0008872
T4 187-194 DiseaseOrPhenotypicFeature denotes MOPD II 0008872
T5 228-240 DiseaseOrPhenotypicFeature denotes microcephaly 0001149
T6 330-350 DiseaseOrPhenotypicFeature denotes primary microcephaly 0016056
T7 351-354 DiseaseOrPhenotypicFeature denotes can 0012833
T8 396-401 DiseaseOrPhenotypicFeature denotes MCPH1 0009617
T9 429-444 DiseaseOrPhenotypicFeature denotes Seckel syndrome 0019342
T10 449-456 DiseaseOrPhenotypicFeature denotes MOPD II 0008872
T11 477-498 DiseaseOrPhenotypicFeature denotes ataxia telangiectasia 0008840
T12 619-624 DiseaseOrPhenotypicFeature denotes MCPH1 0009617