About: Enzyme defects

An Entity of Type: Concept, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Property	Value
dbo:wikiPageID	30048939 (xsd:integer)
dbo:wikiPageRevisionID	833678133 (xsd:integer)
dbp:wikiPageUsesTemplate	dbt:Commons_category
rdf:type	skos:Concept
rdfs:label	Enzyme defects (en)
skos:broader	dbc:Genetic_disorders_by_mechanism dbc:Enzymes
skos:prefLabel	Enzyme defects (en)
prov:wasDerivedFrom	wikipedia-en:Category:Enzyme_defects?oldid=833678133&ns=14
is dbo:wikiPageWikiLink of	dbr:Moynahan_syndrome dbr:Metachondromatosis dbr:Methylenetetrahydrofolate_dehydrogenase_1_deficiency dbr:Hypophosphatasia dbr:Cortisone_reductase_deficiency dbr:RASopathy dbr:Chronic_granulomatous_disease dbr:Calpainopathy dbr:Noonan_syndrome dbr:Noonan_syndrome_with_multiple_lentigines dbr:Incontinentia_pigmenti dbr:Severe_congenital_neutropenia dbr:Neutral_lipid_storage_disease dbr:Neutrophil-specific_granule_deficiency dbr:Walker–Warburg_syndrome dbr:Myeloperoxidase_deficiency dbr:X-linked_recessive_chondrodysplasia_punctata
is dcterms:subject of	dbr:Moynahan_syndrome dbr:Metachondromatosis dbr:Methylenetetrahydrofolate_dehydrogenase_1_deficiency dbr:Hypophosphatasia dbr:Cortisone_reductase_deficiency dbr:RASopathy dbr:Chronic_granulomatous_disease dbr:Calpainopathy dbr:Noonan_syndrome dbr:Noonan_syndrome_with_multiple_lentigines dbr:Incontinentia_pigmenti dbr:Severe_congenital_neutropenia dbr:Neutral_lipid_storage_disease dbr:Neutrophil-specific_granule_deficiency dbr:Walker–Warburg_syndrome dbr:Myeloperoxidase_deficiency dbr:X-linked_recessive_chondrodysplasia_punctata
is skos:broader of	dbc:Defects_of_enzyme_cofactors dbc:Inborn_errors_of_metabolism

This content was extracted from Wikipedia and is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License