About: WS2B

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

WS2B is a putative gene associated with Waardenburg syndrome type 2. It has not yet been isolated from its locus of chromosome 1p21–1p13.3 since it was first reported in 1994.

Property Value
dbo:abstract
  • WS2B هوَ جين مُرتبط بمتلازمة واردينبيرغ. (ar)
  • WS2B is a putative gene associated with Waardenburg syndrome type 2. It has not yet been isolated from its locus of chromosome 1p21–1p13.3 since it was first reported in 1994. (en)
dbo:arm
  • p
dbo:band
  • 21
dbo:chromosome
  • 1
dbo:entrezgene
  • 7488
dbo:hgncid
  • 12794
dbo:locusSupplementaryData
  • -1p13.3
dbo:omim
  • 600193 (xsd:integer)
dbo:symbol
  • WS2B
dbo:wikiPageID
  • 10949697 (xsd:integer)
dbo:wikiPageLength
  • 1903 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID
  • 1003874362 (xsd:integer)
dbo:wikiPageWikiLink
dbp:arm
  • p (en)
dbp:band
  • 21 (xsd:integer)
dbp:chromosome
  • 1 (xsd:integer)
dbp:entrezgene
  • 7488 (xsd:integer)
dbp:hgncid
  • 12794 (xsd:integer)
dbp:locussupplementarydata
  • -1 (xsd:integer)
dbp:name
  • Waardenburg syndrome, type 2B (en)
dbp:omim
  • 600193 (xsd:integer)
dbp:symbol
  • WS2B (en)
dbp:wikiPageUsesTemplate
gold:hypernym
rdf:type
rdfs:comment
  • WS2B هوَ جين مُرتبط بمتلازمة واردينبيرغ. (ar)
  • WS2B is a putative gene associated with Waardenburg syndrome type 2. It has not yet been isolated from its locus of chromosome 1p21–1p13.3 since it was first reported in 1994. (en)
rdfs:label
  • WS2B (ar)
  • WS2B (en)
owl:sameAs
prov:wasDerivedFrom
foaf:isPrimaryTopicOf
is dbo:wikiPageWikiLink of
is foaf:primaryTopic of
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