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18708620
Source:
http://linkedlifedata.com/resource/pubmed/id/18708620
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Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0015272
,
umls-concept:C0020302
,
umls-concept:C0035820
,
umls-concept:C0205225
,
umls-concept:C0439801
,
umls-concept:C0812327
,
umls-concept:C1414668
pubmed:issue
1
pubmed:dateCreated
2009-1-6
pubmed:abstractText
Primary congenital glaucoma (PCG) is an autosomal recessive disorder that has been linked to CYP1B1 mutations. This study was conducted to explore the role of FOXC1, which is involved in anterior segment dysgenesis, in PCG.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7703701
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aryl Hydrocarbon Hydroxylases
,
http://linkedlifedata.com/resource/pubmed/chemical/CYP1B1 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System
,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers
,
http://linkedlifedata.com/resource/pubmed/chemical/FOXC1 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Forkhead Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1552-5783
pubmed:author
pubmed-author:ChakrabartiSubhabrataS
,
pubmed-author:KaurInderjeetI
,
pubmed-author:KaurKiranpreetK
,
pubmed-author:MandalAnil KAK
,
pubmed-author:ParikhRajul SRS
,
pubmed-author:RaoKollu NageswaraKN
,
pubmed-author:ThomasRaviR
pubmed:issnType
Electronic
pubmed:volume
50
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
75-83
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:18708620-Age of Onset
,
pubmed-meshheading:18708620-Anterior Eye Segment
,
pubmed-meshheading:18708620-Aryl Hydrocarbon Hydroxylases
,
pubmed-meshheading:18708620-Cytochrome P-450 Enzyme System
,
pubmed-meshheading:18708620-DNA Primers
,
pubmed-meshheading:18708620-Female
,
pubmed-meshheading:18708620-Forkhead Transcription Factors
,
pubmed-meshheading:18708620-Frameshift Mutation
,
pubmed-meshheading:18708620-Glaucoma
,
pubmed-meshheading:18708620-Humans
,
pubmed-meshheading:18708620-Infant, Newborn
,
pubmed-meshheading:18708620-Male
,
pubmed-meshheading:18708620-Mutation, Missense
,
pubmed-meshheading:18708620-Pedigree
,
pubmed-meshheading:18708620-Polymerase Chain Reaction
pubmed:year
2009
pubmed:articleTitle
The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma.
pubmed:affiliation
Hyderabad Eye Research Foundation, Hyderabad, India. subho@lvpei.org
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't