Item:Q12895: Difference between revisions

Created a new Item: monogenic disease, Human disease
 
Created claim: exact match (P409): http://identifiers.org/doid/DOID:0050177
 
(4 intermediate revisions by the same user not shown)
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / subclass of
 
Property / subclass of: genetic disease / rank
 
Normal rank
Property / has cause
 
Property / has cause: single gene mutation / rank
 
Normal rank
Property / exact match
 
Property / exact match: http://purl.obolibrary.org/obo/DOID_0050177 / rank
 
Normal rank
Property / exact match
 
Property / exact match: http://identifiers.org/doid/DOID:0050177 / rank
 
Normal rank