PRO_ID	Object_term	Object_syny	Modifier	Relation	Ontology_ID	Ontology_term	Relative_to	Interaction_with	Evidence_source	Evidence_code	Taxon	Inferred_from	DB_ID	Date	Assigned_by	Comment
PR:000037700	presenilin-1 sequence variant L286P (human)	hPSEN1/var:L286P|UniProtKB:P49768-1, Leu-286, CHEBI:50342		associated_with_disease_progression	DOID:10652	Alzheimer's disease			Alzforum:psen1-l286p	EXP	NCBITaxon:9606		Alzforum:psen1-l286p	20180510	PRO:DAN	
PR:000037700	presenilin-1 sequence variant L286P (human)	hPSEN1/var:L286P|UniProtKB:P49768-1, Leu-286, CHEBI:50342		associated_with_disease_progression	DOID:9246	cerebral amyloid angiopathy			Alzforum:psen1-l286p	EXP	NCBITaxon:9606		Alzforum:psen1-l286p	20180510	PRO:DAN