2.9.1.2	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26115735&form=6&db=m	Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate.	causal interaction,unassigned	3,0	
2.9.1.2	Brain Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26805434&form=6&db=m	Pontocerebellar hypoplasia type 2D and optic nerve atrophy further expand the spectrum associated with selenoprotein biosynthesis deficiency.	causal interaction,unassigned	4,0	
2.9.1.2	Infections	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26975431&form=6&db=m	Selenoproteins of African trypanosomes are dispensable for parasite survival in a mammalian host.	ongoing research,therapeutic application,unassigned	3,1,0	
2.9.1.2	Hepatitis, Autoimmune	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28690845&form=6&db=m	Diagnostic autoantibodies for autoimmune liver diseases.	causal interaction,unassigned	1,0	
2.9.1.2	Infections	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28810614&form=6&db=m	Evolution of correlation between Helicobacter pylori infection and autoimmune liver disease.	diagnostic usage,unassigned	2,0	
2.9.1.2	Cerebellar Ataxia	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29464431&form=6&db=m	A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxia.	causal interaction,ongoing research,unassigned	2,1,0	
2.9.1.2	Microcephaly	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29464431&form=6&db=m	A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxia.	causal interaction,ongoing research,unassigned	2,1,0	
2.9.1.2	Neurodegenerative Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29709707&form=6&db=m	Consequences of mutations and inborn errors of selenoprotein biosynthesis and functions.	causal interaction,unassigned	4,0