154319

Source:http://linkedlifedata.com/resource/pubmed/id/154319

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0022596, umls-concept:C0025517, umls-concept:C0231335, umls-concept:C0238767, umls-concept:C0268483, umls-concept:C0268487, umls-concept:C0439640, umls-concept:C0439660, umls-concept:C0441748, umls-concept:C0917816
pubmed:issue	75
pubmed:dateCreated	1979-4-25
pubmed:language	ger
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7505238
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine
pubmed:status	MEDLINE
pubmed:issn	0070-427X
pubmed:author	pubmed-author:GallaschGG, pubmed-author:JaegerWW, pubmed-author:PENNS WSW, pubmed-author:SchmidtHH, pubmed-author:SchnyderU WUW
pubmed:issnType	Print
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	649-54
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:154319-Amino Acid Metabolism, Inborn Errors, pubmed-meshheading:154319-Child, pubmed-meshheading:154319-Chromosome Aberrations, pubmed-meshheading:154319-Chromosome Disorders, pubmed-meshheading:154319-Genes, Recessive, pubmed-meshheading:154319-Humans, pubmed-meshheading:154319-Intellectual Disability, pubmed-meshheading:154319-Keratitis, Dendritic, pubmed-meshheading:154319-Keratoderma, Palmoplantar, pubmed-meshheading:154319-Syndrome, pubmed-meshheading:154319-Tyrosine
pubmed:year	1978
pubmed:articleTitle	[Tyrosinemia and Richner-Hanhart syndrome (an autosomal recessive hereditary metabolic disease of childhood with bilateral dendritic pseudokeratitis, keratosis palmaris et plantaris and mental deficiency].
pubmed:publicationType	Journal Article, English Abstract