Preferred Label : Disease_Mapped_To_Gene;
NCIt definition : A role used to assert a direct relationship between a disease, disorder or finding
and a gene. This restriction can be used when a polymorphism or an abnormality in
a gene is either a clinical marker for, a causative event for, or predisposes a subject
to a disease. The domain and range for this role are 'Disease, Disorder or Finding'
and 'Gene', respectively.;
Origin ID : C96816;
UMLS CUI : C3273057;
Semantic type(s)
- role_has_domain
- role_has_range
