18188948

Source:http://linkedlifedata.com/resource/pubmed/id/18188948

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004083, umls-concept:C0026882, umls-concept:C0031437, umls-concept:C0035331, umls-concept:C0039082, umls-concept:C0241764, umls-concept:C1419623
pubmed:dateCreated	2008-1-14
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/EY07003, http://linkedlifedata.com/resource/pubmed/grant/EY07961
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0121103
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Arginine, http://linkedlifedata.com/resource/pubmed/chemical/Eye Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RPGR protein, human
pubmed:status	MEDLINE
pubmed:issn	0065-2598
pubmed:author	pubmed-author:BranhamKariK, pubmed-author:CantrellApril DAD, pubmed-author:IannacconeAlessandroA, pubmed-author:JenningsBarbara JBJ, pubmed-author:OthmanMohammad IMI, pubmed-author:SwaroopAnandA
pubmed:issnType	Print
pubmed:volume	613
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	221-7
pubmed:dateRevised	2009-1-14
pubmed:meshHeading	pubmed-meshheading:18188948-Arginine, pubmed-meshheading:18188948-DNA Mutational Analysis, pubmed-meshheading:18188948-Electroretinography, pubmed-meshheading:18188948-Eye Proteins, pubmed-meshheading:18188948-Female, pubmed-meshheading:18188948-Genetic Diseases, X-Linked, pubmed-meshheading:18188948-Hearing Loss, Sensorineural, pubmed-meshheading:18188948-Heterozygote, pubmed-meshheading:18188948-Humans, pubmed-meshheading:18188948-Male, pubmed-meshheading:18188948-Mutation, Missense, pubmed-meshheading:18188948-Otitis Media, pubmed-meshheading:18188948-Pedigree, pubmed-meshheading:18188948-Phenotype, pubmed-meshheading:18188948-Respiratory Tract Infections, pubmed-meshheading:18188948-Retina, pubmed-meshheading:18188948-Retinitis Pigmentosa, pubmed-meshheading:18188948-Usher Syndromes
pubmed:year	2008
pubmed:articleTitle	Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene.
pubmed:affiliation	Hamilton Eye Institute, Department of Ophthalmology, University of Tennessee Health Science Center, 930 Madison Avenue, Suite 731, Memphis, TN 38163, USA. aiannacc@utmem.edu
pubmed:publicationType	Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural