Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency

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Predicate	Object
rdf:type	diseasome-instance:diseases
rdfs:label	Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency
diseasome-instance:omim	http://bio2rdf.org/omim:250850
diseasome-instance:diseaseS...	diseasome-diseases:551
diseasome-instance:associat...	diseasome-gene:MAT1A, diseasome-gene:MATA1, diseasome-gene:SAMS1
diseasome-instance:class	http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseaseClass/Metabolic
diseasome-instance:chromoso...	http://www4.wiwiss.fu-berlin.de/diseasome/resource/chromosomalLocation/10q22
diseasome-instance:omimPage	http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250850
diseasome-instance:possible...	http://www4.wiwiss.fu-berlin.de/drugbank/resource/drugs/DB00118, http://www4.wiwiss.fu-berlin.de/drugbank/resource/drugs/DB00134
diseasome-instance:name	Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency