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

Source:http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/2679

Statements in which the resource exists.
SubjectPredicateObjectContext
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diseasome-diseases:2679rdfs:labelHypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiencylld:diseasome
diseasome-diseases:2679diseasome-instance:omimhttp://bio2rdf.org/omim:250...lld:diseasome
diseasome-diseases:2679diseasome-instance:diseaseS...diseasome-diseases:551lld:diseasome
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diseasome-diseases:2679diseasome-instance:associat...diseasome-gene:SAMS1lld:diseasome
diseasome-diseases:2679diseasome-instance:classhttp://www4.wiwiss.fu-berli...lld:diseasome
diseasome-diseases:2679diseasome-instance:chromoso...http://www4.wiwiss.fu-berli...lld:diseasome
diseasome-diseases:2679diseasome-instance:omimPagehttp://www.ncbi.nlm.nih.gov...lld:diseasome
diseasome-diseases:2679diseasome-instance:possible...http://www4.wiwiss.fu-berli...lld:diseasome
diseasome-diseases:2679diseasome-instance:possible...http://www4.wiwiss.fu-berli...lld:diseasome
diseasome-diseases:2679diseasome-instance:nameHypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiencylld:diseasome
http://www4.wiwiss.fu-berli...relontology:treatdiseasome-diseases:2679lld:causality
http://www4.wiwiss.fu-berli...relontology:treatdiseasome-diseases:2679lld:causality