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19608540
Source:
http://linkedlifedata.com/resource/pubmed/id/19608540
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0016781
,
umls-concept:C0023745
,
umls-concept:C0031437
,
umls-concept:C0205314
,
umls-concept:C0547040
,
umls-concept:C0679622
,
umls-concept:C1708726
pubmed:issue
12
pubmed:dateCreated
2009-12-3
pubmed:abstractText
To identify the disease locus associated with autosomal dominant Fuchs corneal dystrophy (FCD) in a large family and to compare the progression of severity in families mapped to the FCD1 and FCD2 loci.
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/R01EY016835
,
http://linkedlifedata.com/resource/pubmed/grant/R01HD04260
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7703701
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1552-5783
pubmed:author
pubmed-author:Al-SaifAmrA
,
pubmed-author:DaveyLisaL
,
pubmed-author:EghrariAllen OAO
,
pubmed-author:GottschJohn DJD
,
pubmed-author:KatsanisNicholasN
,
pubmed-author:MeadowsDanielle NDN
,
pubmed-author:RiazuddinS AmerSA
pubmed:issnType
Electronic
pubmed:volume
50
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5667-71
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:19608540-Aged
,
pubmed-meshheading:19608540-Chromosomes, Human, Pair 5
,
pubmed-meshheading:19608540-Female
,
pubmed-meshheading:19608540-Fuchs' Endothelial Dystrophy
,
pubmed-meshheading:19608540-Genetic Linkage
,
pubmed-meshheading:19608540-Genotype
,
pubmed-meshheading:19608540-Humans
,
pubmed-meshheading:19608540-Lod Score
,
pubmed-meshheading:19608540-Male
,
pubmed-meshheading:19608540-Microsatellite Repeats
,
pubmed-meshheading:19608540-Middle Aged
,
pubmed-meshheading:19608540-Pedigree
,
pubmed-meshheading:19608540-Phenotype
,
pubmed-meshheading:19608540-Polymerase Chain Reaction
,
pubmed-meshheading:19608540-Polymorphism, Single Nucleotide
pubmed:year
2009
pubmed:articleTitle
Linkage of a mild late-onset phenotype of Fuchs corneal dystrophy to a novel locus at 5q33.1-q35.2.
pubmed:affiliation
McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't
,
Research Support, N.I.H., Extramural