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- Q17911648 subject Q6939040.
- Q17911648 abstract "Cytochrome b5, form A (gene name CYB5A), is a human microsomal cytochrome b5.Cytochrome b5 is a membrane bound hemoprotein which function as an electron carrier for several membrane bound oxygenases. It has two isoforms produced by alternative splicing. Isoform 1 is bound to the cytoplasmic side of the endoplasmic reticulum. It has a C-terminal transmembrane alpha-helix. Isoform 2 was found in cytoplasm. Defects in CYB5A are the cause of type IV hereditary methemoglobinemia.".
- Q17911648 entrezgene "1528".
- Q17911648 wikiPageWikiLink Q1129238.
- Q17911648 wikiPageWikiLink Q419615.
- Q17911648 wikiPageWikiLink Q5201346.
- Q17911648 wikiPageWikiLink Q547502.
- Q17911648 wikiPageWikiLink Q609809.
- Q17911648 wikiPageWikiLink Q6939040.
- Q17911648 wikiPageWikiLink Q748442.
- Q17911648 wikiPageWikiLink Q79927.
- Q17911648 wikiPageWikiLink Q902628.
- Q17911648 type Biomolecule.
- Q17911648 type Protein.
- Q17911648 type Thing.
- Q17911648 type Q206229.
- Q17911648 type Q8054.
- Q17911648 comment "Cytochrome b5, form A (gene name CYB5A), is a human microsomal cytochrome b5.Cytochrome b5 is a membrane bound hemoprotein which function as an electron carrier for several membrane bound oxygenases. It has two isoforms produced by alternative splicing. Isoform 1 is bound to the cytoplasmic side of the endoplasmic reticulum. It has a C-terminal transmembrane alpha-helix. Isoform 2 was found in cytoplasm. Defects in CYB5A are the cause of type IV hereditary methemoglobinemia.".
- Q17911648 label "Cytochrome b5, type A".