9727204

Source:http://linkedlifedata.com/resource/pubmed/id/9727204

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0005744, umls-concept:C0017337, umls-concept:C0024779, umls-concept:C0033377, umls-concept:C0039082, umls-concept:C0291905, umls-concept:C0332183, umls-concept:C0733755, umls-concept:C1303003, umls-concept:C1419287, umls-concept:C1419317, umls-concept:C1882417, umls-concept:C2828389
pubmed:issue	4
pubmed:dateCreated	1998-11-24
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8709751
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Retinol-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Retinol-Binding Proteins, Cellular
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	0890-8508
pubmed:author	pubmed-author:AmatiPP, pubmed-author:BiscegliaLL, pubmed-author:BonneauDD, pubmed-author:CarelliEE, pubmed-author:GaspariniPP, pubmed-author:PiemonteseM RMR, pubmed-author:PiliaGG, pubmed-author:ZelanteLL, pubmed-author:d'AmbrosioLL
pubmed:issnType	Print
pubmed:volume	12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	255-8
pubmed:dateRevised	2007-11-15
pubmed:meshHeading	pubmed-meshheading:9727204-Blepharophimosis, pubmed-meshheading:9727204-Blepharoptosis, pubmed-meshheading:9727204-Chromosome Mapping, pubmed-meshheading:9727204-Chromosomes, Human, Pair 3, pubmed-meshheading:9727204-Genes, pubmed-meshheading:9727204-Humans, pubmed-meshheading:9727204-Introns, pubmed-meshheading:9727204-Polymorphism, Genetic, pubmed-meshheading:9727204-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:9727204-Retinol-Binding Proteins, pubmed-meshheading:9727204-Retinol-Binding Proteins, Cellular, pubmed-meshheading:9727204-Syndrome
pubmed:year	1998
pubmed:articleTitle	Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome gene.
pubmed:affiliation	Servizio di Genetica Medica, IRCCS-Ospedale CSS, San Giovanni Rotondo, Italy.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't