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PubMed:10200057 JSONTXT

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DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10200057-0#64#69#geners62507329 64-69 geners62507329 denotes P362T
10200057-0#120#135#diseaseC0031485 120-135 diseaseC0031485 denotes phenylketonuria
10200057-0#120#135#diseaseC0751434 120-135 diseaseC0751434 denotes phenylketonuria
10200057-5#37#42#geners62516101 747-752 geners62516101 denotes V388M
10200057-5#61#64#diseaseC0031485 771-774 diseaseC0031485 denotes PKU
10200057-5#61#64#diseaseC0751434 771-774 diseaseC0751434 denotes PKU
64#69#geners62507329120#135#diseaseC0031485 10200057-0#64#69#geners62507329 10200057-0#120#135#diseaseC0031485 associated_with P362T,phenylketonuria
64#69#geners62507329120#135#diseaseC0751434 10200057-0#64#69#geners62507329 10200057-0#120#135#diseaseC0751434 associated_with P362T,phenylketonuria
37#42#geners6251610161#64#diseaseC0031485 10200057-5#37#42#geners62516101 10200057-5#61#64#diseaseC0031485 associated_with V388M,PKU
37#42#geners6251610161#64#diseaseC0751434 10200057-5#37#42#geners62516101 10200057-5#61#64#diseaseC0751434 associated_with V388M,PKU

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10200057-0#38#41#gene5053 38-41 gene5053 denotes PAH
10200057-0#120#135#diseaseC0031485 120-135 diseaseC0031485 denotes phenylketonuria
10200057-0#120#135#diseaseC0751434 120-135 diseaseC0751434 denotes phenylketonuria
38#41#gene5053120#135#diseaseC0031485 10200057-0#38#41#gene5053 10200057-0#120#135#diseaseC0031485 associated_with PAH,phenylketonuria
38#41#gene5053120#135#diseaseC0751434 10200057-0#38#41#gene5053 10200057-0#120#135#diseaseC0751434 associated_with PAH,phenylketonuria

DisGeNET

Id Subject Object Predicate Lexical cue
T0 173-176 gene:5053 denotes PKU
T1 201-216 disease:C0019247 denotes genetic disease
R1 T0 T1 associated_with PKU,genetic disease

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 556-564 HP_0001289 denotes confused