hasPhenotype

URI: https://gptkb.org/prop/hasPhenotype
188 triples
GPTKB property
Alternative names (5)
associated phenotype • associatedWithPhenotype • has phenotype • phenotype • phenotypes
Random triples
Subject Object
gptkb:OMIM:160790 chronic pulmonary disease
gptkb:Silver-Russell_syndrome_(mouse_model) craniofacial abnormalities
gptkb:Fanconi_anemia,_complementation_group_D2 skeletal anomalies
gptkb:Beckwith-Wiedemann_syndrome_(mouse_model) increased tumor risk
gptkb:beta-thalassemia_(in_mouse_models) gptkb:anemia
gptkb:BALB/cJ prone to developing lung tumors
gptkb:E._coli_B_strain_REL606 Ara- (arabinose negative)
gptkb:AGTR2_gene X-linked mental retardation
gptkb:OMIM:607709 muscle atrophy
gptkb:Drosophila_lethal(2)_giant_larvae_(lgl) lethality in homozygous mutants
gptkb:Nr1h3 impaired lipid homeostasis
gptkb:BALB/cJ high IgE response
gptkb:beta-thalassemia_(in_mouse_models) iron overload
gptkb:subcortical_band_heterotopia variable cognitive impairment
gptkb:FUS_transgenic_mouse muscle weakness
gptkb:BALB/cAnNCrl albino
gptkb:FBgn0003461 wingless phenotype
gptkb:Temple-Baraitser_syndrome broad nasal bridge
gptkb:Oncomouse high incidence of cancer
gptkb:OMIM:160790 elevated sweat chloride