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4118080
Source:
http://linkedlifedata.com/resource/pubmed/id/4118080
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51
)
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0031485
,
umls-concept:C0349590
,
umls-concept:C0751435
,
umls-concept:C1457869
,
umls-concept:C1521991
pubmed:issue
5377
pubmed:dateCreated
1973-2-2
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0410462
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Carbon Isotopes
,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes
,
http://linkedlifedata.com/resource/pubmed/chemical/Lysophosphatidylcholines
,
http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine
,
http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine Hydroxylase
,
http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0028-0836
pubmed:author
pubmed-author:FriedmanP APA
,
pubmed-author:HoodC HCH
,
pubmed-author:KaufmanSS
pubmed:issnType
Print
pubmed:day
17
pubmed:volume
240
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
157-9
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:4118080-Amino Acid Metabolism, Inborn Errors
,
pubmed-meshheading:4118080-Animals
,
pubmed-meshheading:4118080-Carbon Isotopes
,
pubmed-meshheading:4118080-Epitopes
,
pubmed-meshheading:4118080-Genes
,
pubmed-meshheading:4118080-Genes, Regulator
,
pubmed-meshheading:4118080-Humans
,
pubmed-meshheading:4118080-Immunodiffusion
,
pubmed-meshheading:4118080-Kinetics
,
pubmed-meshheading:4118080-Liver
,
pubmed-meshheading:4118080-Lysophosphatidylcholines
,
pubmed-meshheading:4118080-Mutation
,
pubmed-meshheading:4118080-Phenylalanine
,
pubmed-meshheading:4118080-Phenylalanine Hydroxylase
,
pubmed-meshheading:4118080-Phenylketonurias
,
pubmed-meshheading:4118080-Rats
,
pubmed-meshheading:4118080-Sheep
,
pubmed-meshheading:4118080-Tyrosine
pubmed:year
1972
pubmed:articleTitle
Nature of the molecular defect in phenylketonuria and hyperphenylalaninaemia.
pubmed:publicationType
Journal Article