Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q17917742> ?p ?o }
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- Q17917742 abstract "Eyes absent homolog 1 is a protein that in humans is encoded by the EYA1 gene.This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Four transcript variants encoding three distinct isoforms have been identified for this gene.".
- Q17917742 entrezgene "2138".
- Q17917742 wikiPageWikiLink Q18031509.
- Q17917742 wikiPageWikiLink Q7187.
- Q17917742 wikiPageWikiLink Q8054.
- Q17917742 wikiPageWikiLink Q896177.
- Q17917742 type Biomolecule.
- Q17917742 type Protein.
- Q17917742 type Thing.
- Q17917742 type Q206229.
- Q17917742 type Q8054.
- Q17917742 comment "Eyes absent homolog 1 is a protein that in humans is encoded by the EYA1 gene.This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies.".
- Q17917742 label "EYA1".