|
#
|
Concept name
|
Type
|
Relation
|
Support
|
Score
|
|
1
|
Heparin, Low-Molecular-Weight
|
Compound
|
Known
|
Explain
|
13.82500
|
|
2
|
Sinus Thrombosis, Intracranial
|
Disease
|
Known
|
Explain
|
9.06983
|
|
3
|
Glycosaminoglycans
|
Compound
|
Known
|
Explain
|
7.92353
|
|
4
|
FGF19 gene
|
Gene
|
Known
|
Explain
|
3.62380
|
|
5
|
FGF5 gene
|
Gene
|
Known
|
Explain
|
3.45472
|
|
6
|
Thrombosis
|
Disease
|
Known
|
Explain
|
3.20079
|
|
7
|
FGF4 gene
|
Gene
|
Known
|
Explain
|
2.91085
|
|
8
|
Dalteparin
|
Compound
|
Inferred
|
Explain
|
2.40112
|
|
9
|
FGFR4 gene
|
Gene
|
Known
|
Explain
|
2.26327
|
|
10
|
Thrombocytopenia
|
Disease
|
Known
|
Explain
|
2.22006
|
|
11
|
Vasculitis
|
Disease
|
Known
|
Explain
|
2.06600
|
|
12
|
FGF1 gene
|
Gene
|
Known
|
Explain
|
1.50488
|
|
13
|
F2 gene
|
Gene
|
Known
|
Explain
|
1.25448
|
|
14
|
F2R gene
|
Gene
|
Known
|
Explain
|
1.10393
|
|
15
|
FGFR1 gene
|
Gene
|
Known
|
Explain
|
0.76595
|
|
16
|
Liver Cirrhosis, Experimental
|
Disease
|
Known
|
Explain
|
0.76436
|
|
17
|
FGF2 gene
|
Gene
|
Known
|
Explain
|
0.74272
|
|
18
|
Intracranial Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.71394
|
|
19
|
FGF10 gene
|
Gene
|
Known
|
Explain
|
0.68277
|
|
20
|
FGFR2 gene
|
Gene
|
Known
|
Explain
|
0.60304
|
|
21
|
ABCC1 gene
|
Gene
|
Known
|
Explain
|
0.51517
|
|
22
|
Chondroitin
|
Compound
|
Inferred
|
Explain
|
0.45497
|
|
23
|
Keratan Sulfate
|
Compound
|
Inferred
|
Explain
|
0.35814
|
|
24
|
Heparitin Sulfate
|
Compound
|
Inferred
|
Explain
|
0.33966
|
|
25
|
Intracranial Embolism and Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.22980
|
|
26
|
Alzheimer's Disease
|
Disease
|
Inferred
|
Explain
|
0.17800
|
|
27
|
Warfarin
|
Compound
|
Inferred
|
Explain
|
0.15887
|
|
28
|
Hyaluronic Acid
|
Compound
|
Inferred
|
Explain
|
0.14743
|
|
29
|
IDUA gene
|
Gene
|
Inferred
|
Explain
|
0.11258
|
|
30
|
Polysaccharides
|
Compound
|
Inferred
|
Explain
|
0.08568
|
|
31
|
Dermatan Sulfate
|
Compound
|
Inferred
|
Explain
|
0.07443
|
|
32
|
Chondroitin Sulfates
|
Compound
|
Inferred
|
Explain
|
0.07018
|
|
33
|
MTHFR gene
|
Gene
|
Inferred
|
Explain
|
0.05588
|
|
34
|
Thromboembolism
|
Disease
|
Inferred
|
Explain
|
0.05306
|
|
35
|
Aloxiprimum
|
Compound
|
Inferred
|
Explain
|
0.04105
|
|
36
|
argatroban
|
Compound
|
Inferred
|
Explain
|
0.03318
|
|
37
|
Interleukin 1/heparin-binding growth factor
|
Domain
|
Inferred
|
Explain
|
0.02958
|
|
38
|
Carotid Artery Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.02923
|
|
39
|
Heparin-binding growth factor/Fibroblast growth factor
|
Domain
|
Inferred
|
Explain
|
0.02878
|
|
40
|
fibroblast growth factor receptor binding
|
Function
|
Inferred
|
Explain
|
0.02742
|
|
41
|
Cytokine, IL-1-like
|
Domain
|
Inferred
|
Explain
|
0.02157
|
|
42
|
bivalirudin
|
Compound
|
Inferred
|
Explain
|
0.02057
|
|
43
|
fibroblast growth factor receptor signaling pathway
|
Function
|
Inferred
|
Explain
|
0.02001
|
|
44
|
VASCULITIS, LYMPHOCYTIC, CUTANEOUS SMALL VESSEL
|
Disease
|
Inferred
|
Explain
|
0.01868
|
|
45
|
VASCULITIS, LYMPHOCYTIC, NODULAR
|
Disease
|
Inferred
|
Explain
|
0.01868
|
|
46
|
Embolism and Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.01691
|
|
47
|
CHST6 gene
|
Gene
|
Inferred
|
Explain
|
0.01544
|
|
48
|
B3GNT2 gene
|
Gene
|
Inferred
|
Explain
|
0.01450
|
|
49
|
Melanoma - Homo sapiens (human)
|
Pathway
|
Inferred
|
Explain
|
0.01390
|
|
50
|
HBW 023
|
Compound
|
Inferred
|
Explain
|
0.01347
|
|
51
|
Arteritis
|
Disease
|
Inferred
|
Explain
|
0.01229
|
|
52
|
Cerebrovascular Disorders
|
Disease
|
Inferred
|
Explain
|
0.01221
|
|
53
|
Vasculitis, Central Nervous System
|
Disease
|
Inferred
|
Explain
|
0.01174
|
|
54
|
Venous Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.01136
|
|
55
|
Phlebitis
|
Disease
|
Inferred
|
Explain
|
0.01128
|
|
56
|
Vasculitis Adverse Event
|
Disease
|
Inferred
|
Explain
|
0.01109
|
|
57
|
Hypersensitivity vasculitis
|
Disease
|
Inferred
|
Explain
|
0.01088
|
|
58
|
Heparan Sulfate Proteoglycans
|
Compound
|
Inferred
|
Explain
|
0.01074
|
|
59
|
Lymphocyte
|
Other
|
Inferred
|
Explain
|
0.01029
|
|
60
|
Shwartzman Phenomenon
|
Disease
|
Inferred
|
Explain
|
0.00988
|
|
61
|
Aortitis
|
Disease
|
Inferred
|
Explain
|
0.00988
|
|
62
|
insulin receptor signaling pathway
|
Function
|
Inferred
|
Explain
|
0.00982
|
|
63
|
Henoch-Schoenlein Purpura
|
Disease
|
Inferred
|
Explain
|
0.00980
|
|
64
|
Malignant Atrophic Papulosis
|
Disease
|
Inferred
|
Explain
|
0.00972
|
|
65
|
Retinal Vasculitis
|
Disease
|
Inferred
|
Explain
|
0.00965
|
|
66
|
Thromboangiitis Obliterans
|
Disease
|
Inferred
|
Explain
|
0.00962
|
|
67
|
Systemic Vasculitis
|
Disease
|
Inferred
|
Explain
|
0.00937
|
|
68
|
Thrombophilia
|
Disease
|
Inferred
|
Explain
|
0.00914
|
|
69
|
Regulation of actin cytoskeleton - Homo sapiens (human)
|
Pathway
|
Inferred
|
Explain
|
0.00897
|
|
70
|
FGF8 gene
|
Gene
|
Inferred
|
Explain
|
0.00853
|
|
71
|
FGF7 gene
|
Gene
|
Inferred
|
Explain
|
0.00824
|
|
72
|
PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY
|
Disease
|
Inferred
|
Explain
|
0.00818
|
|
73
|
Mucocutaneous Lymph Node Syndrome
|
Disease
|
Inferred
|
Explain
|
0.00812
|
|
74
|
positive regulation of ERK1 and ERK2 cascade
|
Function
|
Inferred
|
Explain
|
0.00796
|
|
75
|
THROMBOCYTOPENIA 2 (disorder)
|
Disease
|
Inferred
|
Explain
|
0.00779
|
|
76
|
Skin Diseases, Vascular
|
Disease
|
Inferred
|
Explain
|
0.00770
|
|
77
|
Thrombotic Microangiopathies
|
Disease
|
Inferred
|
Explain
|
0.00751
|
|
78
|
Blood Platelet Disorders
|
Disease
|
Inferred
|
Explain
|
0.00742
|
|
79
|
THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE
|
Disease
|
Inferred
|
Explain
|
0.00694
|
|
80
|
GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA
|
Disease
|
Inferred
|
Explain
|
0.00693
|
|
81
|
Coronary Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.00680
|
|
82
|
Fibroblast growth factor, 15/19/21
|
Domain
|
Inferred
|
Explain
|
0.00679
|
|
83
|
growth factor activity
|
Function
|
Inferred
|
Explain
|
0.00676
|
|
84
|
DK PHOCOMELIA SYNDROME
|
Disease
|
Inferred
|
Explain
|
0.00668
|
|
85
|
Gestodene
|
Compound
|
Inferred
|
Explain
|
0.00665
|
|
86
|
PROC gene
|
Gene
|
Inferred
|
Explain
|
0.00664
|
|
87
|
positive regulation of cell division
|
Function
|
Inferred
|
Explain
|
0.00661
|
|
88
|
Neonatal alloimmune thrombocytopenia
|
Disease
|
Inferred
|
Explain
|
0.00652
|
|
89
|
Jacobsen syndrome
|
Disease
|
Inferred
|
Explain
|
0.00651
|
|
90
|
SERPIND1 gene
|
Gene
|
Inferred
|
Explain
|
0.00649
|
|
91
|
Ticlopidine Hydrochloride
|
Compound
|
Inferred
|
Explain
|
0.00635
|
|
92
|
THROMBOCYTOPENIA 1 (disorder)
|
Disease
|
Inferred
|
Explain
|
0.00628
|
|
93
|
MAPK Signaling Pathway Pathway
|
Function
|
Inferred
|
Explain
|
0.00627
|
|
94
|
MASTL gene
|
Gene
|
Inferred
|
Explain
|
0.00614
|
|
95
|
Behcet Syndrome
|
Disease
|
Inferred
|
Explain
|
0.00599
|
|
96
|
Stimulation of Cell Proliferation
|
Function
|
Inferred
|
Explain
|
0.00595
|
|
97
|
B4GALT1 gene
|
Gene
|
Inferred
|
Explain
|
0.00553
|
|
98
|
Oculovestibuloauditory syndrome
|
Disease
|
Inferred
|
Explain
|
0.00540
|
|
99
|
Immune Complex Diseases
|
Disease
|
Inferred
|
Explain
|
0.00540
|
|
100
|
THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCED GLOBIN SYNTHESIS
|
Disease
|
Inferred
|
Explain
|
0.00525
|