Matches in DBpedia 2014 for { <http://dbpedia.org/resource/DYM> ?p ?o. }
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- DYM abstract "Dymeclin is a protein that in humans is encoded by the DYM gene.This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation.".
- DYM entrezgene "54808".
- DYM wikiPageID "15219613".
- DYM wikiPageRevisionID "434518307".
- DYM hasPhotoCollection DYM.
- DYM requireManualInspection "no".
- DYM summaryText "This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen dysplasia and Smith-McCort dysplasia, which involve both skeletal defects and mental retardation.".
- DYM updateCitations "yes".
- DYM updatePage "yes".
- DYM updateProteinBox "yes".
- DYM updateSummary "yes".
- DYM type Biomolecule.
- DYM type Protein.
- DYM type BiologicalObject.
- DYM comment "Dymeclin is a protein that in humans is encoded by the DYM gene.This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation.".
- DYM label "DYM".
- DYM sameAs m.03hm8rh.
- DYM sameAs Q5206842.
- DYM sameAs Q5206842.
- DYM sameAs DYM.
- DYM wasDerivedFrom DYM?oldid=434518307.
- DYM isPrimaryTopicOf DYM.