> top > projects > HP-phenotype > docs > PubMed:9489699 > annotations
HP-phenotype  

PubMed:9489699 JSONTXT 11 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue hp_id
T1 94-105 Phenotype denotes heterotopia HP:0002282
T2 110-123 Phenotype denotes lissencephaly HP:0001339
T3 141-144 Phenotype denotes LIS HP:0001339
T4 159-186 Phenotype denotes neuronal migration disorder HP:0002269
T5 268-279 Phenotype denotes heterotopia HP:0002282
T6 292-303 Phenotype denotes heterotopia HP:0002282
T7 338-351 Phenotype denotes lissencephaly HP:0001339
T8 353-356 Phenotype denotes LIS HP:0001339
T9 379-387 Phenotype denotes epilepsy HP:0001250
T10 392-412 Phenotype denotes cognitive impairment HP:0100543
T11 589-592 Phenotype denotes LIS HP:0001339
T12 899-912 Phenotype denotes lissencephaly HP:0001339
T13 917-928 Phenotype denotes heterotopia HP:0002282