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http://dbpedia.org/class/yago/WikicatGeneticDisordersWithNoOMIM
About: http://dbpedia.org/class/yago/WikicatGeneticDisordersWithNoOMIM
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About:
http://dbpedia.org/class/yago/WikicatGeneticDisordersWithNoOMIM
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
rdfs:
subClassOf
yago
:GeneticDisease114151139
owl:
equivalentClass
yago-res
:wikicat_Genetic_disorders_with_no_OMIM
is
rdf:
type
of
dbr
:Amelanism
dbr
:Partial_monosomy_13q
dbr
:Hyperphenylalaninemia
dbr
:Bhaskar–Jagannathan_syndrome
dbr
:Interleukin-1_receptor–associated_kinase_4_deficiency
dbr
:Lethal_white_syndrome
dbr
:Leucism
dbr
:Singleton_Merten_syndrome
dbr
:Aniridia_ataxia_renal_agenesis_psychomotor_retardation
dbr
:Erondu–Cymet_syndrome
dbr
:Erythrism
dbr
:Scott_syndrome
dbr
:Congenital_dyserythropoietic_anemia
dbr
:Congenital_dyserythropoietic_anemia_type_I
dbr
:Congenital_dyserythropoietic_anemia_type_II
dbr
:Congenital_dyserythropoietic_anemia_type_III
dbr
:Congenital_dyserythropoietic_anemia_type_IV
dbr
:Congenital_fibrosis_of_the_extraocular_muscles
dbr
:Cooks_syndrome
dbr
:Crouzonodermoskeletal_syndrome
dbr
:Lachiewicz–Sibley_syndrome
dbr
:Nullisomic
dbr
:Batten_disease
dbr
:Benjamin_syndrome
dbr
:Lethal_arthrogryposis_with_anterior_horn_cell_disease
dbr
:Snatiation
dbr
:Dentinogenesis_imperfecta
dbr
:Hemoglobin_variants
dbr
:Microorchidism
dbr
:Ayazi_syndrome
dbr
:8p23.1_duplication_syndrome
dbr
:Acytosiosis
dbr
:GMS_syndrome
dbr
:2q37_deletion_syndrome
dbr
:Banti's_syndrome
dbr
:Central_nervous_system_cavernous_hemangioma
dbr
:Chromosome_15q_partial_deletion
dbr
:Chromosome_15q_trisomy
dbr
:Isodicentric_15
dbr
:Xanthochromism
dbr
:Hereditary_spastic_paraplegia
dbr
:Bare_lymphocyte_syndrome_2
dbr
:Tetrasomy_18p
dbr
:Tetrasomy_9p
dbr
:Fibular_hemimelia
dbr
:Cerebellar_hypoplasia
dbr
:Gulf_War_syndrome
dbr
:Distal_Trisomy_10q
dbr
:Management_of_hair_loss
dbr
:Zamzam–Sheriff–Phillips_syndrome
dbr
:Polychromia
dbr
:Impossible_syndrome
dbr
:SADDAN
dbr
:Van_Goethem_syndrome
dbr
:Male-pattern_hair_loss
dbr
:Ring_chromosome_14_syndrome
dbr
:Ring_chromosome_20_syndrome
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