Bio2Vec

BIO-KNOWLEDGE-GRAPH

A knowledge graph of biological entities such as genes, gene functions, diseases, phenotypes and chemicals. Embeddings are generated with Walking RDF and OWL method.

MIR499B

ID: http://www.ncbi.nlm.nih.gov/gene/100616134

Type: http://bio2vec.net/ontology/gene

Label: MIR499B

Synonyms: MIR499B, MIR499A, hsa-mir-499b, microRNA 499b, hsa-mir-499a, microRNA 499a

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

MIR499B

http://www.ncbi.nlm.nih.gov/gene/100616134
TRBV5-1

http://www.ncbi.nlm.nih.gov/gene/28614
no_name

http://www.ncbi.nlm.nih.gov/gene/100128356
ENPP7P13

http://www.ncbi.nlm.nih.gov/gene/104644205
hereditary spastic paraplegia

DOID:2476
DEFB105A

http://www.ncbi.nlm.nih.gov/gene/245908
sacral spinal canal and spinal cord meningioma

DOID:8203
chronic metabolic polyneuropathy

DOID:7441
CELIAC11

http://www.ncbi.nlm.nih.gov/gene/100188873
MIR520D

http://www.ncbi.nlm.nih.gov/gene/574482
C1orf127

http://www.ncbi.nlm.nih.gov/gene/148345
MIR1231

http://www.ncbi.nlm.nih.gov/gene/100302158
PDB4

http://www.ncbi.nlm.nih.gov/gene/94003
Pelizaeus-Merzbacher disease

DOID:3210
Aicardi syndrome

DOID:8461
SCA18

http://www.ncbi.nlm.nih.gov/gene/94008
spastic quadriplegia

DOID:10970
autosomal dominant microcephaly

DOID:14725
SPG19

http://www.ncbi.nlm.nih.gov/gene/140907
ETL2

http://www.ncbi.nlm.nih.gov/gene/619399
hyperkalemic periodic paralysis

DOID:14451
OR2W5

http://www.ncbi.nlm.nih.gov/gene/441932
HAS2-AS1

http://www.ncbi.nlm.nih.gov/gene/594842
CLQTL1

http://www.ncbi.nlm.nih.gov/gene/54501
MIR1181

http://www.ncbi.nlm.nih.gov/gene/100302213
SPG29

http://www.ncbi.nlm.nih.gov/gene/619379
MT2P1

http://www.ncbi.nlm.nih.gov/gene/4503
MIR1273C

http://www.ncbi.nlm.nih.gov/gene/100422821
LGMD1G

http://www.ncbi.nlm.nih.gov/gene/553991
MIR935

http://www.ncbi.nlm.nih.gov/gene/100126325
IBD21

http://www.ncbi.nlm.nih.gov/gene/100192312
striatonigral degeneration

DOID:4751
delta chain disease

DOID:0060129
SPG36

http://www.ncbi.nlm.nih.gov/gene/791228
ERVK-24

http://www.ncbi.nlm.nih.gov/gene/100862684
Mobius syndrome

DOID:13501
IGLL2P

http://www.ncbi.nlm.nih.gov/gene/3544
GLC1J

http://www.ncbi.nlm.nih.gov/gene/574078
spastic hemiplegia

DOID:10967
DEFB107A

http://www.ncbi.nlm.nih.gov/gene/245910
familial periodic paralysis

DOID:1029
no_name

http://www.ncbi.nlm.nih.gov/gene/100500805
spinal meninges cancer

DOID:7224
LOC102724334

http://www.ncbi.nlm.nih.gov/gene/102724334
CELIAC12

http://www.ncbi.nlm.nih.gov/gene/100188874
PABPC1P2

http://www.ncbi.nlm.nih.gov/gene/728773
frontal convexity meningioma

DOID:8000
primary amebic meningoencephalitis

DOID:0050242
CHEBI:250624

http://aber-owl.net/drug/CID044325607
Andersen-Tawil syndrome

DOID:0050434
CHEMBL92470

http://aber-owl.net/drug/CID044325531
spinal accessory nerve neoplasm

DOID:337
meningioma by site

DOID:4142
LINC00951

http://www.ncbi.nlm.nih.gov/gene/401260
DEFA7P

http://www.ncbi.nlm.nih.gov/gene/724067
mucopolysaccharidosis VI

DOID:12800
generalized convulsive epilepsy

DOID:7724
atrophic muscular disease

DOID:913
SureCN6443713

http://aber-owl.net/drug/CID118420249
no_name

DOID:7225
MIR602

http://www.ncbi.nlm.nih.gov/gene/693187
hereditary multiple exostoses

DOID:206
CADASIL

DOID:13945
congenital disorder

DOID:759
pediatric germ cell cancer

DOID:6053
pediatric CNS embryonal cell carcinoma

DOID:7231
pituitary hypoplasia

DOID:7378
centronuclear myopathy

DOID:14717
spasmodic dystonia

DOID:0050844
orofaciodigital syndrome

DOID:4501
SLC2A3P1

http://www.ncbi.nlm.nih.gov/gene/100128062
Reduced volume of central subdivision of bed nucleus of stria terminalis

HP:0030797
Alexander disease

DOID:4252
IGHV3-76

http://www.ncbi.nlm.nih.gov/gene/28406
DBET

http://www.ncbi.nlm.nih.gov/gene/100419743
no_name

DOID:1640
malignant neoplasm of short bones of lower limb

DOID:10151
oppositional defiant disorder

DOID:0050856
benign neonatal seizures

DOID:14264
gangliocytoma

DOID:2426
benign breast adenomyoepithelioma

DOID:1641
SPG16

http://www.ncbi.nlm.nih.gov/gene/57760
SLEN2

http://www.ncbi.nlm.nih.gov/gene/192679
Meige syndrome

DOID:3982
LOC100499484-C9ORF174

http://www.ncbi.nlm.nih.gov/gene/57653
orbital cancer

DOID:4143
arteriolosclerosis

DOID:5162
recurrent ovarian germ cell neoplasm

DOID:7855
disease of biological process

DOID:344
CELIAC8

http://www.ncbi.nlm.nih.gov/gene/100188870
spinal cord primitive neuroectodermal neoplasm

DOID:6872
abetalipoproteinemia

DOID:1386
no_name

DOID:8595
Bilateral basal ganglia lesions

HP:0007146
Gerstmann-Straussler-Scheinker syndrome

DOID:4249
no_name

DOID:10984
oculocerebrorenal syndrome

DOID:1056
resectable bile duct cancer

DOID:5933
no_name

DOID:0050121
childhood immature teratoma of ovary

DOID:7037

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