Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q18031407> ?p ?o }
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- Q18031407 subject Q8482243.
- Q18031407 abstract "Protein SCO1 homolog, mitochondrial is a protein that in humans is encoded by the SCO1 gene.Mutations in both SCO1 and SCO2 are associated with distinct clinical phenotypes as well as tissue-specific cytochrome c oxidase deficiency. SCO1 localizes predominantly to blood vessels, whereas SCO2 is barely detectable. Expression of SCO2 is also much higher than that of SCO1 in muscle tissue, while SCO1 is expressed at higher levels in liver tissue than SCO2.".
- Q18031407 entrezgene "6341".
- Q18031407 wikiPageWikiLink Q103824.
- Q18031407 wikiPageWikiLink Q13048280.
- Q18031407 wikiPageWikiLink Q1364740.
- Q18031407 wikiPageWikiLink Q14819361.
- Q18031407 wikiPageWikiLink Q1501412.
- Q18031407 wikiPageWikiLink Q150839.
- Q18031407 wikiPageWikiLink Q16335184.
- Q18031407 wikiPageWikiLink Q1658004.
- Q18031407 wikiPageWikiLink Q18034942.
- Q18031407 wikiPageWikiLink Q1815019.
- Q18031407 wikiPageWikiLink Q20951084.
- Q18031407 wikiPageWikiLink Q213907.
- Q18031407 wikiPageWikiLink Q245341.
- Q18031407 wikiPageWikiLink Q306116.
- Q18031407 wikiPageWikiLink Q3285695.
- Q18031407 wikiPageWikiLink Q333203.
- Q18031407 wikiPageWikiLink Q444351.
- Q18031407 wikiPageWikiLink Q4896390.
- Q18031407 wikiPageWikiLink Q5910791.
- Q18031407 wikiPageWikiLink Q608256.
- Q18031407 wikiPageWikiLink Q631521.
- Q18031407 wikiPageWikiLink Q6531938.
- Q18031407 wikiPageWikiLink Q692536.
- Q18031407 wikiPageWikiLink Q7096029.
- Q18031407 wikiPageWikiLink Q7168698.
- Q18031407 wikiPageWikiLink Q7181398.
- Q18031407 wikiPageWikiLink Q7187.
- Q18031407 wikiPageWikiLink Q7365.
- Q18031407 wikiPageWikiLink Q8054.
- Q18031407 wikiPageWikiLink Q8482243.
- Q18031407 wikiPageWikiLink Q849994.
- Q18031407 wikiPageWikiLink Q9368.
- Q18031407 type Biomolecule.
- Q18031407 type Protein.
- Q18031407 type Thing.
- Q18031407 type Q206229.
- Q18031407 type Q8054.
- Q18031407 comment "Protein SCO1 homolog, mitochondrial is a protein that in humans is encoded by the SCO1 gene.Mutations in both SCO1 and SCO2 are associated with distinct clinical phenotypes as well as tissue-specific cytochrome c oxidase deficiency. SCO1 localizes predominantly to blood vessels, whereas SCO2 is barely detectable. Expression of SCO2 is also much higher than that of SCO1 in muscle tissue, while SCO1 is expressed at higher levels in liver tissue than SCO2.".
- Q18031407 label "SCO1".