2.5.1.6	Acquired Immunodeficiency Syndrome	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19653152&form=6&db=m	[Do ethical guidelines provide assistance in clinical practice?]	causal interaction,unassigned	1,0	
2.5.1.6	Adenocarcinoma	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23588207&form=6&db=m	Polyamine and methionine adenosyltransferase 2A crosstalk in human colon and liver cancer.	causal interaction,diagnostic usage,ongoing research,therapeutic application	1,3,4,1	
2.5.1.6	adenosine kinase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=27671891&form=6&db=m	Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders.	causal interaction,therapeutic application,unassigned	4,1,0	
2.5.1.6	Alzheimer Disease	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7549452&form=6&db=m	Decreased methionine adenosyltransferase activity in erythrocytes of patients with dementia disorders.	causal interaction,diagnostic usage,ongoing research,unassigned	3,2,2,0	
2.5.1.6	Alzheimer Disease	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8872870&form=6&db=m	Influence of vitamin B12 on brain methionine adenosyltransferase activity in senile dementia of the Alzheimer's type.	causal interaction,diagnostic usage,ongoing research,unassigned	1,1,4,0	
2.5.1.6	Alzheimer Disease	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28450540&form=6&db=m	APLP1 Is a Synaptic Cell Adhesion Molecule, Supporting Maintenance of Dendritic Spines and Basal Synaptic Transmission.	causal interaction,unassigned	3,0	
2.5.1.6	Amyotrophic Lateral Sclerosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=10415148&form=6&db=m	Methionine adenosyltransferase activity in erythrocytes and spinal cord of patients with sporadic amyotrophic lateral sclerosis.	ongoing research,unassigned	1,0	
2.5.1.6	Aortic Aneurysm, Thoracic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25557781&form=6&db=m	MAT2A mutations predispose individuals to thoracic aortic aneurysms.	causal interaction,unassigned	2,0	
2.5.1.6	Aortic Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25557781&form=6&db=m	MAT2A mutations predispose individuals to thoracic aortic aneurysms.	causal interaction,unassigned	2,0	
2.5.1.6	Asthma	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25258128&form=6&db=m	Do family physicians choose self-assessment activities based on what they know or don't know?	therapeutic application,unassigned	1,0