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- Q200985 subject Q6853484.
- Q200985 subject Q6902466.
- Q200985 subject Q7215445.
- Q200985 subject Q8620826.
- Q200985 subject Q8750387.
- Q200985 abstract "Hartnup disease (also known as "pellagra-like dermatosis" and "Hartnup disorder") is an autosomal recessive metabolic disorder affecting the absorption of nonpolar amino acids (particularly tryptophan that can be, in turn, converted into serotonin, melatonin, and niacin). Niacin is a precursor to nicotinamide, a necessary component of NAD+.The causative gene, SLC6A19, is located on chromosome 5.".
- Q200985 icd10 "E72.0".
- Q200985 icd9 "270.0".
- Q200985 meshId "D006250".
- Q200985 omim "234500".
- Q200985 thumbnail L-tryptophan-skeletal.png?width=300.
- Q200985 wikiPageExternalLink 001201.htm.
- Q200985 wikiPageWikiLink Q11090.
- Q200985 wikiPageWikiLink Q1149042.
- Q200985 wikiPageWikiLink Q1149046.
- Q200985 wikiPageWikiLink Q13048280.
- Q200985 wikiPageWikiLink Q134658.
- Q200985 wikiPageWikiLink Q142943.
- Q200985 wikiPageWikiLink Q1442923.
- Q200985 wikiPageWikiLink Q167934.
- Q200985 wikiPageWikiLink Q18055372.
- Q200985 wikiPageWikiLink Q180912.
- Q200985 wikiPageWikiLink Q181003.
- Q200985 wikiPageWikiLink Q186380.
- Q200985 wikiPageWikiLink Q192423.
- Q200985 wikiPageWikiLink Q220989.
- Q200985 wikiPageWikiLink Q221441.
- Q200985 wikiPageWikiLink Q229256.
- Q200985 wikiPageWikiLink Q2351083.
- Q200985 wikiPageWikiLink Q28775.
- Q200985 wikiPageWikiLink Q319541.
- Q200985 wikiPageWikiLink Q40878.
- Q200985 wikiPageWikiLink Q4746435.
- Q200985 wikiPageWikiLink Q4746440.
- Q200985 wikiPageWikiLink Q5754639.
- Q200985 wikiPageWikiLink Q6531938.
- Q200985 wikiPageWikiLink Q6853484.
- Q200985 wikiPageWikiLink Q6902466.
- Q200985 wikiPageWikiLink Q7215445.
- Q200985 wikiPageWikiLink Q774347.
- Q200985 wikiPageWikiLink Q8066.
- Q200985 wikiPageWikiLink Q827658.
- Q200985 wikiPageWikiLink Q83030.
- Q200985 wikiPageWikiLink Q840741.
- Q200985 wikiPageWikiLink Q859142.
- Q200985 wikiPageWikiLink Q8620826.
- Q200985 wikiPageWikiLink Q8750387.
- Q200985 wikiPageWikiLink Q9377.
- Q200985 wikiPageWikiLink Q949302.
- Q200985 icd "270".
- Q200985 icd "E72.0".
- Q200985 meshid "D006250".
- Q200985 name "Hartnup disease".
- Q200985 omim "234500".
- Q200985 type Disease.
- Q200985 type Thing.
- Q200985 type Q12136.
- Q200985 comment "Hartnup disease (also known as "pellagra-like dermatosis" and "Hartnup disorder") is an autosomal recessive metabolic disorder affecting the absorption of nonpolar amino acids (particularly tryptophan that can be, in turn, converted into serotonin, melatonin, and niacin). Niacin is a precursor to nicotinamide, a necessary component of NAD+.The causative gene, SLC6A19, is located on chromosome 5.".
- Q200985 label "Hartnup disease".
- Q200985 depiction L-tryptophan-skeletal.png.
- Q200985 name "Hartnup disease".