Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q1112752> ?p ?o }
Showing triples 1 to 26 of
26
with 100 triples per page.
- Q1112752 subject Q7215483.
- Q1112752 abstract "Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.".
- Q1112752 icd10 "Q87.1".
- Q1112752 meshId "D009456".
- Q1112752 omim "193520".
- Q1112752 wikiPageWikiLink Q1418735.
- Q1112752 wikiPageWikiLink Q200779.
- Q1112752 wikiPageWikiLink Q20782771.
- Q1112752 wikiPageWikiLink Q246809.
- Q1112752 wikiPageWikiLink Q277606.
- Q1112752 wikiPageWikiLink Q635339.
- Q1112752 wikiPageWikiLink Q7215483.
- Q1112752 wikiPageWikiLink Q7502090.
- Q1112752 wikiPageWikiLink Q7616509.
- Q1112752 wikiPageWikiLink Q7987389.
- Q1112752 wikiPageWikiLink Q80726.
- Q1112752 icd "Q87.1".
- Q1112752 meshid "D009456".
- Q1112752 name "Watson syndrome".
- Q1112752 omim "193520".
- Q1112752 type Disease.
- Q1112752 type Thing.
- Q1112752 type Q12136.
- Q1112752 comment "Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.".
- Q1112752 label "Watson syndrome".
- Q1112752 name "Watson syndrome".