Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/BBS2> ?p ?o }
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- BBS2 abstract "Bardet-Biedl syndrome 2 protein is a protein that in humans is encoded by the BBS2 gene.This gene encodes a protein of unknown function. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 2. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation, and mental retardation.".
- BBS2 entrezgene "583".
- BBS2 wikiPageExternalLink br.fcgi?book=gene&part=bbs.
- BBS2 wikiPageID "14881242".
- BBS2 wikiPageLength "7778".
- BBS2 wikiPageOutDegree "3".
- BBS2 wikiPageRevisionID "673166209".
- BBS2 wikiPageWikiLink Bardet–Biedl_syndrome.
- BBS2 wikiPageWikiLink Gene.
- BBS2 wikiPageWikiLink Protein.
- BBS2 wikiPageWikiLinkText "BBS2".
- BBS2 requireManualInspection "no".
- BBS2 summaryText "This gene encodes a protein of unknown function. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 2. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation, and mental retardation.".
- BBS2 updateCitations "yes".
- BBS2 updatePage "yes".
- BBS2 updateProteinBox "yes".
- BBS2 updateSummary "yes".
- BBS2 wikiPageUsesTemplate Template:Ciliary_proteins.
- BBS2 wikiPageUsesTemplate Template:Cite_journal.
- BBS2 wikiPageUsesTemplate Template:Gene-16-stub.
- BBS2 wikiPageUsesTemplate Template:PBB.
- BBS2 wikiPageUsesTemplate Template:PBB_Controls.
- BBS2 wikiPageUsesTemplate Template:PBB_Further_reading.
- BBS2 wikiPageUsesTemplate Template:PBB_Summary.
- BBS2 wikiPageUsesTemplate Template:Refbegin.
- BBS2 wikiPageUsesTemplate Template:Refend.
- BBS2 wikiPageUsesTemplate Template:Reflist.
- BBS2 hypernym Protein.
- BBS2 type Biomolecule.
- BBS2 type Protein.
- BBS2 type Thing.
- BBS2 type Q206229.
- BBS2 type Q8054.
- BBS2 comment "Bardet-Biedl syndrome 2 protein is a protein that in humans is encoded by the BBS2 gene.This gene encodes a protein of unknown function. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 2. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation, and mental retardation.".
- BBS2 label "BBS2".
- BBS2 sameAs Q17838063.
- BBS2 sameAs m.03h07kf.
- BBS2 sameAs Q17838063.
- BBS2 wasDerivedFrom BBS2?oldid=673166209.
- BBS2 isPrimaryTopicOf BBS2.