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18247295
Source:
http://linkedlifedata.com/resource/pubmed/id/18247295
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53
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0015576
,
umls-concept:C0026882
,
umls-concept:C0028738
,
umls-concept:C0152035
,
umls-concept:C0332240
,
umls-concept:C1744681
,
umls-concept:C1825315
pubmed:issue
1
pubmed:dateCreated
2008-2-5
pubmed:abstractText
To study the mutation of FRMD7 gene in a Chinese family with congenital idiopathic nystagmus.
pubmed:language
chi
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9425197
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Cytoskeletal Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/FRMD7 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1003-9406
pubmed:author
pubmed-author:CuiLi-hongLH
,
pubmed-author:LiNing-dongND
,
pubmed-author:MaHui-zhiHZ
,
pubmed-author:WangLi-mingLM
,
pubmed-author:YueYi-yingYY
,
pubmed-author:ZhangLi-lingLL
,
pubmed-author:ZhaoKan-xingKX
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
11-4
pubmed:meshHeading
pubmed-meshheading:18247295-Asian Continental Ancestry Group
,
pubmed-meshheading:18247295-Base Sequence
,
pubmed-meshheading:18247295-Cytoskeletal Proteins
,
pubmed-meshheading:18247295-Exons
,
pubmed-meshheading:18247295-Family
,
pubmed-meshheading:18247295-Female
,
pubmed-meshheading:18247295-Genome, Human
,
pubmed-meshheading:18247295-Genomics
,
pubmed-meshheading:18247295-Humans
,
pubmed-meshheading:18247295-Male
,
pubmed-meshheading:18247295-Membrane Proteins
,
pubmed-meshheading:18247295-Microsatellite Repeats
,
pubmed-meshheading:18247295-Mutation
,
pubmed-meshheading:18247295-Nystagmus, Congenital
,
pubmed-meshheading:18247295-Pedigree
,
pubmed-meshheading:18247295-Sequence Analysis, DNA
pubmed:year
2008
pubmed:articleTitle
[The G990T mutation of the FRMD7 gene in a Chinese family with congenital idiopathic nystagmus].
pubmed:affiliation
Department of Ophthalmic Molecular Genetics, Tianjin Eye Hospital, Tianjin, People's Republic of China.
pubmed:publicationType
Journal Article
,
English Abstract