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PubMed:25708779 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 188-215 HP_0000707 denotes neurodevelopmental disorder
T2 250-258 HP_0001417 denotes X-linked
T3 286-316 HP_0010864 denotes severe intellectual disability
T4 293-316 HP_0001249 denotes intellectual disability
T5 318-336 HP_0100022 denotes movement disorders
T6 342-350 HP_0000717 denotes autistic
T7 821-834 HP_0001427 denotes mitochondrial
T8 1117-1130 HP_0001427 denotes mitochondrial
T9 1202-1215 HP_0001427 denotes mitochondrial
T10 1752-1765 HP_0001427 denotes mitochondrial
T11 1933-1946 HP_0001427 denotes mitochondrial
T12 2069-2082 HP_0001427 denotes mitochondrial
T13 2198-2211 HP_0001427 denotes mitochondrial

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
25708779-1#106#111#gene4204 259-264 gene4204 denotes MECP2
25708779-1#35#62#diseaseC1535926 188-215 diseaseC1535926 denotes neurodevelopmental disorder
25708779-1#133#163#diseaseC0036857 286-316 diseaseC0036857 denotes severe intellectual disability
25708779-1#189#197#diseaseC0004352 342-350 diseaseC0004352 denotes autistic
25708779-3#112#117#gene4204 565-570 gene4204 denotes MeCP2
25708779-3#188#191#diseaseC0035372 641-644 diseaseC0035372 denotes RTT
106#111#gene420435#62#diseaseC1535926 25708779-1#106#111#gene4204 25708779-1#35#62#diseaseC1535926 associated_with MECP2,neurodevelopmental disorder
106#111#gene4204133#163#diseaseC0036857 25708779-1#106#111#gene4204 25708779-1#133#163#diseaseC0036857 associated_with MECP2,severe intellectual disability
106#111#gene4204189#197#diseaseC0004352 25708779-1#106#111#gene4204 25708779-1#189#197#diseaseC0004352 associated_with MECP2,autistic
112#117#gene4204188#191#diseaseC0035372 25708779-3#112#117#gene4204 25708779-3#188#191#diseaseC0035372 associated_with MeCP2,RTT