Matches in DBpedia 2014 for { <http://dbpedia.org/resource/FBN1> ?p ?o. }
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- FBN1 abstract "Fibrillin-1 is a protein that in humans is encoded by the FBN1 gene, located on chromosome 15.This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.".
- FBN1 entrezgene "2200".
- FBN1 wikiPageExternalLink br.fcgi?book=gene&part=marfan.
- FBN1 wikiPageID "14076409".
- FBN1 wikiPageRevisionID "591289511".
- FBN1 hasPhotoCollection FBN1.
- FBN1 requireManualInspection "no".
- FBN1 updateCitations "yes".
- FBN1 updatePage "yes".
- FBN1 updateProteinBox "yes".
- FBN1 updateSummary "no".
- FBN1 type Biomolecule.
- FBN1 type Protein.
- FBN1 type BiologicalObject.
- FBN1 comment "Fibrillin-1 is a protein that in humans is encoded by the FBN1 gene, located on chromosome 15.This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body.".
- FBN1 label "FBN1".
- FBN1 label "FBN1".
- FBN1 label "Fibrilina 1".
- FBN1 label "Fibrilline 1".
- FBN1 label "إف بي إن 1".
- FBN1 sameAs Fibrilina_1.
- FBN1 sameAs Fibrilline_1.
- FBN1 sameAs FBN1.
- FBN1 sameAs FBN1.
- FBN1 sameAs FBN1.
- FBN1 sameAs m.03cstm7.
- FBN1 sameAs Q2909661.
- FBN1 sameAs Q2909661.
- FBN1 sameAs FBN1.
- FBN1 sameAs MFS1.
- FBN1 wasDerivedFrom FBN1?oldid=591289511.
- FBN1 isPrimaryTopicOf FBN1.