Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)
0.700 CausalMutation disease CLINVAR
LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)
0.700 Biomarker disease CTD_human
LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)
0.700 GeneticVariation disease CLINVAR
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
0.450 Biomarker group HPO
CUI: C0026848
Disease: Myopathy
Myopathy
0.110 Biomarker group HPO
CUI: C0086543
Disease: Cataract
Cataract
0.100 Biomarker disease HPO
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
0.100 Biomarker phenotype HPO
Creatine phosphokinase serum increased
0.100 Biomarker phenotype HPO
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness
0.100 Biomarker phenotype HPO
CUI: C0427064
Disease: Pelvic girdle weakness
Pelvic girdle weakness
0.100 Biomarker phenotype HPO
CUI: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy
0.100 Biomarker phenotype HPO
Decreased movement range in interphalangeal joints
0.100 Biomarker phenotype HPO
CUI: C1853932
Disease: Rimmed vacuoles on biopsy
Rimmed vacuoles on biopsy
0.100 Biomarker phenotype HPO
CUI: C1854494
Disease: Slow progression
Slow progression
0.100 Biomarker phenotype HPO
CUI: C1866013
Disease: Proximal upper limb amyotrophy
Proximal upper limb amyotrophy
0.100 Biomarker phenotype HPO
CUI: C4024731
Disease: Flexion limitation of toes
Flexion limitation of toes
0.100 Biomarker phenotype HPO
CUI: C0019348
Disease: Herpes Simplex Infections
Herpes Simplex Infections
0.010 Biomarker group BEFREE 2 cells with herpes simplex virus type 1 (HSV-1) leads to a reorganization of antigens associated with both the small and heterogeneous nuclear ribonucleoprotein complexes (snRNP and hnRNP). 2824525 1987
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.030 Biomarker disease BEFREE Antibodies to other hnRNP proteins (A1, A2, and B) have been previously found in patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and mixed connective tissue disease (MCTD). 8843857 1996
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 Biomarker disease BEFREE Antibodies to other hnRNP proteins (A1, A2, and B) have been previously found in patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and mixed connective tissue disease (MCTD). 8843857 1996
CUI: C0026272
Disease: Mixed Connective Tissue Disease
Mixed Connective Tissue Disease
0.010 Biomarker disease BEFREE Antibodies to other hnRNP proteins (A1, A2, and B) have been previously found in patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and mixed connective tissue disease (MCTD). 8843857 1996
CUI: C0017638
Disease: Glioma
Glioma
0.010 AlteredExpression disease BEFREE These data indicate that hnRNP A2 is the Glut1 AURE binding protein whose cytoplasmic expression in gliomas is associated with translational repression and mRNA instability. 10441480 1999
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
0.010 AlteredExpression disease BEFREE Using this approach, we also identified the other major Glut1 3'UTR RNA binding activity as hnRNP L. Stimuli (hypoxia and hypoglycemia) which increase Glut1 mRNA stability selectively decreased polysomal levels of hnRNP A2 and L. Immunoprecipitation demonstrated that hnRNP A2 and L exist as a complex in vivo. 10441480 1999
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
MYOTONIC DYSTROPHY 1
0.010 Biomarker disease BEFREE Using a combination of indirect immunofluorescence to detect endogenous proteins and overexpression of proteins with green fluorescent protein (GFP) tags we have shown that CUG-BP and hnRNP C do not co-localise with expanded repeat foci in DM1 cell lines. 11433021 2001
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.090 Biomarker group BEFREE This paper briefly reviews four topics related to mechanisms of action of tea polyphenols: (I) identification of the genes commonly affected by EGCG, as demonstrated by Clontech's Atlas cDNA Expression Array; (II) the significance of heterogeneous nuclear ribonucleoprotein B1 (hnRNP B1) as a new biomarker for early detection of lung cancer, and inhibition of its expression by EGCG; (III) the synergistic or additive effects of EGCG with the cancer preventive agents, sulindac and tamoxifen, on induction of apoptosis in PC-9 cells and on inhibition of intestinal tumor development in multiple intestinal neoplasia (Min) mice; (IV) the results of a 10 year prospective cohort study demonstrating the effectiveness of daily consumption of green tea in preventing cancer, and a prototype study for developing green tea beverage as cancer preventive. 11506822 2001
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.080 Biomarker group BEFREE This paper briefly reviews four topics related to mechanisms of action of tea polyphenols: (I) identification of the genes commonly affected by EGCG, as demonstrated by Clontech's Atlas cDNA Expression Array; (II) the significance of heterogeneous nuclear ribonucleoprotein B1 (hnRNP B1) as a new biomarker for early detection of lung cancer, and inhibition of its expression by EGCG; (III) the synergistic or additive effects of EGCG with the cancer preventive agents, sulindac and tamoxifen, on induction of apoptosis in PC-9 cells and on inhibition of intestinal tumor development in multiple intestinal neoplasia (Min) mice; (IV) the results of a 10 year prospective cohort study demonstrating the effectiveness of daily consumption of green tea in preventing cancer, and a prototype study for developing green tea beverage as cancer preventive. 11506822 2001