> top > docs > PubMed:22516612 > annotations

PubMed:22516612 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET

Id Subject Object Predicate Lexical cue
T0 217-224 gene:8659 denotes ALDH4A1
T1 67-90 disease:C2931835 denotes Type II hyperprolinemia
T2 375-382 gene:8659 denotes HsP5CDH
T3 418-433 disease:C0268528 denotes hyperprolinemia
T4 368-373 gene:8659 denotes P5CDH
T5 418-433 disease:C0268529 denotes hyperprolinemia
T6 375-382 gene:8659 denotes HsP5CDH
T7 418-433 disease:C0268529 denotes hyperprolinemia
T8 368-373 gene:8659 denotes P5CDH
T9 418-433 disease:C0268528 denotes hyperprolinemia
R1 T0 T1 associated_with ALDH4A1,Type II hyperprolinemia
R2 T2 T3 associated_with HsP5CDH,hyperprolinemia
R3 T4 T5 associated_with P5CDH,hyperprolinemia
R4 T6 T7 associated_with HsP5CDH,hyperprolinemia
R5 T8 T9 associated_with P5CDH,hyperprolinemia

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 75-90 HP_0008358 denotes hyperprolinemia
T2 97-116 HP_0000007 denotes autosomal recessive
T3 418-433 HP_0008358 denotes hyperprolinemia

Allie

Id Subject Object Predicate Lexical cue
SS1_22516612_1_0 152-194 expanded denotes Δ(1)-pyrroline-5-carboxylate dehydrogenase
SS2_22516612_1_0 196-201 abbr denotes P5CDH
AE1_22516612_1_0 SS1_22516612_1_0 SS2_22516612_1_0 abbreviatedTo Δ(1)-pyrroline-5-carboxylate dehydrogenase,P5CDH

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
22516612-2#134#147#geners137852937 457-470 geners137852937 denotes Ser352 to Leu
22516612-2#95#110#diseaseC0268528 418-433 diseaseC0268528 denotes hyperprolinemia
134#147#geners13785293795#110#diseaseC0268528 22516612-2#134#147#geners137852937 22516612-2#95#110#diseaseC0268528 associated_with Ser352 to Leu,hyperprolinemia

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
22516612-1#129#134#gene8659 196-201 gene8659 denotes P5CDH
22516612-1#150#157#gene8659 217-224 gene8659 denotes ALDH4A1
22516612-1#0#23#diseaseC2931835 67-90 diseaseC2931835 denotes Type II hyperprolinemia
22516612-1#30#58#diseaseC3899988 97-125 diseaseC3899988 denotes autosomal recessive disorder
22516612-1#0#23#diseaseC2931835 67-90 diseaseC2931835 denotes Type II hyperprolinemia
22516612-1#30#58#diseaseC3899988 97-125 diseaseC3899988 denotes autosomal recessive disorder
22516612-2#45#50#gene8659 368-373 gene8659 denotes P5CDH
22516612-2#52#59#gene8659 375-382 gene8659 denotes HsP5CDH
22516612-2#95#110#diseaseC0268528 418-433 diseaseC0268528 denotes hyperprolinemia
129#134#gene86590#23#diseaseC2931835 22516612-1#129#134#gene8659 22516612-1#0#23#diseaseC2931835 associated_with P5CDH,Type II hyperprolinemia
129#134#gene865930#58#diseaseC3899988 22516612-1#129#134#gene8659 22516612-1#30#58#diseaseC3899988 associated_with P5CDH,autosomal recessive disorder
129#134#gene86590#23#diseaseC2931835 22516612-1#129#134#gene8659 22516612-1#0#23#diseaseC2931835 associated_with P5CDH,Type II hyperprolinemia
129#134#gene865930#58#diseaseC3899988 22516612-1#129#134#gene8659 22516612-1#30#58#diseaseC3899988 associated_with P5CDH,autosomal recessive disorder
150#157#gene86590#23#diseaseC2931835 22516612-1#150#157#gene8659 22516612-1#0#23#diseaseC2931835 associated_with ALDH4A1,Type II hyperprolinemia
150#157#gene865930#58#diseaseC3899988 22516612-1#150#157#gene8659 22516612-1#30#58#diseaseC3899988 associated_with ALDH4A1,autosomal recessive disorder
150#157#gene86590#23#diseaseC2931835 22516612-1#150#157#gene8659 22516612-1#0#23#diseaseC2931835 associated_with ALDH4A1,Type II hyperprolinemia
150#157#gene865930#58#diseaseC3899988 22516612-1#150#157#gene8659 22516612-1#30#58#diseaseC3899988 associated_with ALDH4A1,autosomal recessive disorder
45#50#gene865995#110#diseaseC0268528 22516612-2#45#50#gene8659 22516612-2#95#110#diseaseC0268528 associated_with P5CDH,hyperprolinemia
52#59#gene865995#110#diseaseC0268528 22516612-2#52#59#gene8659 22516612-2#95#110#diseaseC0268528 associated_with HsP5CDH,hyperprolinemia