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PubMed:9489699 JSONTXT

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DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
9489699-3#101#113#gene1641 515-527 gene1641 denotes Doublecortin
9489699-3#175#178#diseaseC0266463 589-592 diseaseC0266463 denotes LIS
101#113#gene1641175#178#diseaseC0266463 9489699-3#101#113#gene1641 9489699-3#175#178#diseaseC0266463 associated_with Doublecortin,LIS

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 74-105 Disease denotes subcortical laminar heterotopia http://purl.obolibrary.org/obo/MONDO_0011830|http://purl.obolibrary.org/obo/MONDO_0020491
T3 110-123 Disease denotes lissencephaly http://purl.obolibrary.org/obo/MONDO_0018838
T4 141-144 Disease denotes LIS http://purl.obolibrary.org/obo/MONDO_0018838
T5 248-279 Disease denotes subcortical laminar heterotopia http://purl.obolibrary.org/obo/MONDO_0011830|http://purl.obolibrary.org/obo/MONDO_0020491
T7 287-303 Disease denotes band heterotopia http://purl.obolibrary.org/obo/MONDO_0020491
T8 308-321 Disease denotes double cortex http://purl.obolibrary.org/obo/MONDO_0020491
T9 338-351 Disease denotes lissencephaly http://purl.obolibrary.org/obo/MONDO_0018838
T10 353-356 Disease denotes LIS http://purl.obolibrary.org/obo/MONDO_0018838
T11 379-387 Disease denotes epilepsy http://purl.obolibrary.org/obo/MONDO_0005027
T12 589-592 Disease denotes LIS http://purl.obolibrary.org/obo/MONDO_0018838
T13 899-912 Disease denotes lissencephaly http://purl.obolibrary.org/obo/MONDO_0018838

Anatomy-MAT

Id Subject Object Predicate Lexical cue mat_id
T1 361-366 Body_part denotes males http://purl.obolibrary.org/obo/MAT_0000029
T2 793-798 Body_part denotes brain http://purl.obolibrary.org/obo/MAT_0000098

HP-phenotype

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

Anatomy-UBERON

Id Subject Object Predicate Lexical cue uberon_id
T1 214-231 Body_part denotes layered neocortex http://purl.obolibrary.org/obo/UBERON_0002301
T2 315-321 Body_part denotes cortex http://purl.obolibrary.org/obo/UBERON_0001851
T3 670-677 Body_part denotes segment http://purl.obolibrary.org/obo/UBERON_0000914
T4 793-798 Body_part denotes brain http://purl.obolibrary.org/obo/UBERON_0000955|http://purl.obolibrary.org/obo/UBERON_6110636
T6 993-999 Body_part denotes neuron http://purl.obolibrary.org/obo/CL_0000540

CL-cell

Id Subject Object Predicate Lexical cue cl_id
T1 30-38 Cell denotes neuronal http://purl.obolibrary.org/obo/CL:0000540
T2 159-167 Cell denotes neuronal http://purl.obolibrary.org/obo/CL:0000540
T3 287-291 Cell denotes band http://purl.obolibrary.org/obo/CL:0000560
T4 828-835 Cell denotes neurons http://purl.obolibrary.org/obo/CL:0000540
T5 993-999 Cell denotes neuron http://purl.obolibrary.org/obo/CL:0000540