undefined method 'sourcedb' for nil

PubMed:11683913 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	152-157	gene:860	denotes	Cbfa1
T1	218-238	disease:C0686761	denotes	lack of ossification
T2	114-119	gene:860	denotes	Runx2
T3	218-238	disease:C0686761	denotes	lack of ossification
T4	1056-1061	gene:4488	denotes	P148H
T5	1070-1098	disease:C1858160	denotes	Boston-type craniosynostosis
T6	1050-1054	gene:4488	denotes	Msx2
T7	1070-1098	disease:C1858160	denotes	Boston-type craniosynostosis
R1	T0	T1	associated_with	Cbfa1,lack of ossification
R2	T2	T3	associated_with	Runx2,lack of ossification
R3	T4	T5	associated_with	P148H,Boston-type craniosynostosis
R4	T6	T7	associated_with	Msx2,Boston-type craniosynostosis

DisGeNET5_variant_disease

Id	Subject	Object	Predicate	Lexical cue
11683913-7#63#68#geners104893895	1056-1061	geners104893895	denotes	P148H
11683913-7#77#105#diseaseC1858160	1070-1098	diseaseC1858160	denotes	Boston-type craniosynostosis
63#68#geners10489389577#105#diseaseC1858160	11683913-7#63#68#geners104893895	11683913-7#77#105#diseaseC1858160	associated_with	P148H,Boston-type craniosynostosis

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
11683913-7#57#61#gene4488	1050-1054	gene4488	denotes	Msx2
11683913-7#63#68#gene4488	1056-1061	gene4488	denotes	P148H
11683913-7#77#105#diseaseC1858160	1070-1098	diseaseC1858160	denotes	Boston-type craniosynostosis
57#61#gene448877#105#diseaseC1858160	11683913-7#57#61#gene4488	11683913-7#77#105#diseaseC1858160	associated_with	Msx2,Boston-type craniosynostosis
63#68#gene448877#105#diseaseC1858160	11683913-7#63#68#gene4488	11683913-7#77#105#diseaseC1858160	associated_with	P148H,Boston-type craniosynostosis