> top > docs > PubMed:10072044 > annotations

PubMed:10072044 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
10072044-1#128#133#geners759304648 185-190 geners759304648 denotes G654A
10072044-1#0#28#diseaseC1628319 57-85 diseaseC1628319 denotes Gelsolin-related amyloidosis
128#133#geners7593046480#28#diseaseC1628319 10072044-1#128#133#geners759304648 10072044-1#0#28#diseaseC1628319 associated_with G654A,Gelsolin-related amyloidosis

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10072044-0#0#8#gene2934 500-514 gene2934 denotes G654A gelsolin
10072044-0#28#55#diseaseC0085220 791-1247 diseaseC0085220 denotes ctive for apolipoprotein E (ApoE), alpha1-antichymotrypsin (alpha1-ACT), and cystatin C (Cys C). Cerebral perivascular fibrinogen immunoreactivity was occasionally noted. The patients showed posterior column degeneration and diffuse loss of myelin in the centrum semiovale with perivascular accentuation. Postmortem magnetic resonance imaging, performed on 1 patient, showed white matter lesions, colocalizing with the histological abnormalities. Our study
10072044-1#143#151#gene2934 200-208 gene2934 denotes gelsolin
10072044-1#0#28#diseaseC1628319 57-85 diseaseC1628319 denotes Gelsolin-related amyloidosis
10072044-3#215#223#gene2934 616-624 gene2934 denotes gelsolin
10072044-3#232#239#diseaseC0002726 633-640 diseaseC0002726 denotes amyloid
10072044-3#241#245#diseaseC0002726 642-646 diseaseC0002726 denotes AGel
0#8#gene293428#55#diseaseC0085220 10072044-0#0#8#gene2934 10072044-0#28#55#diseaseC0085220 associated_with G654A gelsolin,"ctive for apolipoprotein E (ApoE), alpha1-antichymotrypsin (alpha1-ACT), and cystatin C (Cys C). Cerebral perivascular fibrinogen immunoreactivity was occasionally noted. The patients showed posterior column degeneration and diffuse loss of myelin in the centrum semiovale with perivascular accentuation. Postmortem magnetic resonance imaging, performed on 1 patient, showed white matter lesions, colocalizing with the histological abnormalities. Our study"
143#151#gene29340#28#diseaseC1628319 10072044-1#143#151#gene2934 10072044-1#0#28#diseaseC1628319 associated_with gelsolin,Gelsolin-related amyloidosis
215#223#gene2934232#239#diseaseC0002726 10072044-3#215#223#gene2934 10072044-3#232#239#diseaseC0002726 associated_with gelsolin,amyloid
215#223#gene2934241#245#diseaseC0002726 10072044-3#215#223#gene2934 10072044-3#241#245#diseaseC0002726 associated_with gelsolin,AGel

DisGeNET

Id Subject Object Predicate Lexical cue
T0 0-8 gene:2934 denotes Gelsolin
T1 28-55 disease:C0085220 denotes cerebral amyloid angiopathy
R1 T0 T1 associated_with Gelsolin,cerebral amyloid angiopathy

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 74-85 HP_0011034 denotes amyloidosis
T2 96-107 HP_0011034 denotes amyloidosis
T3 224-236 HP_0010628 denotes Facial palsy
T4 243-264 HP_0009830 denotes peripheral neuropathy
T5 270-295 HP_0001149 denotes corneal lattice dystrophy
T6 329-341 HP_0001283 denotes bulbar palsy
T7 343-349 HP_0001251 denotes ataxia
T8 343-357 HP_0002066 denotes ataxia of gait
T9 369-389 HP_0100543 denotes cognitive impairment
T10 567-576 HP_0002858 denotes meningeal
T11 577-584 HP_0011034 denotes amyloid
T12 633-640 HP_0011034 denotes amyloid
T13 746-753 HP_0011034 denotes amyloid
T14 1325-1333 HP_0002858 denotes meninges
T15 1434-1445 HP_0011034 denotes amyloidosis