1.16.1.10	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27236917&form=6&db=m	Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy.	causal interaction,unassigned	1,0	
1.16.1.10	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27239025&form=6&db=m	Epileptic encephalopathy with continuous spike-and-wave during sleep maps to a homozygous truncating mutation in AMPA receptor component FRRS1L.	causal interaction,unassigned	1,0	
1.16.1.10	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29086067&form=6&db=m	Emerging Monogenic Complex Hyperkinetic Disorders.	causal interaction,unassigned	4,0	
1.16.1.10	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32928027&form=6&db=m	Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.	causal interaction,unassigned	4,0	
1.16.1.10	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34483011&form=6&db=m	Clonic seizures, continuous spikes-and-waves during slow sleep, choreoathetosis and response to sulthiame in a child with FRRS1L encephalopathy.	causal interaction,therapeutic application,unassigned	4,4,0	
1.16.1.10	Drug Resistant Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32928027&form=6&db=m	Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.	causal interaction,unassigned	4,0	
1.16.1.10	Drug Resistant Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34483011&form=6&db=m	Clonic seizures, continuous spikes-and-waves during slow sleep, choreoathetosis and response to sulthiame in a child with FRRS1L encephalopathy.	causal interaction,therapeutic application,unassigned	4,4,0	
1.16.1.10	Dyskinesias	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32928027&form=6&db=m	Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.	causal interaction,unassigned	4,0	
1.16.1.10	Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27236917&form=6&db=m	Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy.	causal interaction,unassigned	1,0	
1.16.1.10	Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29276473&form=6&db=m	Ferric Chelate Reductase 1 Like Protein (FRRS1L) Associates with Dynein Vesicles and Regulates Glutamatergic Synaptic Transmission.	causal interaction,therapeutic application,unassigned	3,1,0	
1.16.1.10	Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32928027&form=6&db=m	Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.	causal interaction,unassigned	4,0	
1.16.1.10	Hyperkinesis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29086067&form=6&db=m	Emerging Monogenic Complex Hyperkinetic Disorders.	causal interaction,unassigned	4,0	
1.16.1.10	Hyperkinesis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32928027&form=6&db=m	Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.	causal interaction,unassigned	4,0	
1.16.1.10	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28675162&form=6&db=m	AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability.	causal interaction,unassigned	3,0	
1.16.1.10	Language Development Disorders	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28675162&form=6&db=m	AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability.	causal interaction,unassigned	3,0	
1.16.1.10	Lennox Gastaut Syndrome	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32928027&form=6&db=m	Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.	causal interaction,unassigned	4,0	
1.16.1.10	Movement Disorders	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32928027&form=6&db=m	Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.	causal interaction,unassigned	4,0	
1.16.1.10	Nervous System Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27236917&form=6&db=m	Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy.	causal interaction,unassigned	1,0	
1.16.1.10	Seizures	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34483011&form=6&db=m	Clonic seizures, continuous spikes-and-waves during slow sleep, choreoathetosis and response to sulthiame in a child with FRRS1L encephalopathy.	causal interaction,therapeutic application,unassigned	4,4,0	
1.16.1.10	Spasms, Infantile	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32928027&form=6&db=m	Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements.	causal interaction,unassigned	4,0