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18079686
Source:
http://linkedlifedata.com/resource/pubmed/id/18079686
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0158551
,
umls-concept:C0205314
,
umls-concept:C0205419
,
umls-concept:C0679622
,
umls-concept:C1273518
,
umls-concept:C1442161
pubmed:dateCreated
2007-12-14
pubmed:abstractText
To investigate a novel deletion variant of gammaD-crystallin (CRYGD) identified in a Chinese family with nuclear congenital cataract.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9605351
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CRYGD protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Crystallins
,
http://linkedlifedata.com/resource/pubmed/chemical/gamma-Crystallins
pubmed:status
MEDLINE
pubmed:issn
1090-0535
pubmed:author
pubmed-author:FanDorothy Shu-PingDS
,
pubmed-author:LamDennis Shun-ChiuDS
,
pubmed-author:PangChi-PuiCP
,
pubmed-author:TamPancy Oi-SinPO
,
pubmed-author:YamGary Hin-FaiGH
,
pubmed-author:ZhangLi-YunLY
pubmed:issnType
Electronic
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2096-104
pubmed:dateRevised
2010-5-21
pubmed:meshHeading
pubmed-meshheading:18079686-Asian Continental Ancestry Group
,
pubmed-meshheading:18079686-Cataract
,
pubmed-meshheading:18079686-Chromosome Mapping
,
pubmed-meshheading:18079686-Crystallins
,
pubmed-meshheading:18079686-Female
,
pubmed-meshheading:18079686-Frameshift Mutation
,
pubmed-meshheading:18079686-Gene Deletion
,
pubmed-meshheading:18079686-Genes, Dominant
,
pubmed-meshheading:18079686-Genetic Variation
,
pubmed-meshheading:18079686-Humans
,
pubmed-meshheading:18079686-Lens Nucleus, Crystalline
,
pubmed-meshheading:18079686-Male
,
pubmed-meshheading:18079686-Multigene Family
,
pubmed-meshheading:18079686-Solubility
,
pubmed-meshheading:18079686-Tissue Distribution
,
pubmed-meshheading:18079686-gamma-Crystallins
pubmed:year
2007
pubmed:articleTitle
A novel deletion variant of gammaD-crystallin responsible for congenital nuclear cataract.
pubmed:affiliation
Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong, China.
pubmed:publicationType
Journal Article