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18443316
Source:
http://linkedlifedata.com/resource/pubmed/id/18443316
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58
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0008059
,
umls-concept:C0017337
,
umls-concept:C0018787
,
umls-concept:C0026882
,
umls-concept:C0205314
,
umls-concept:C0215223
,
umls-concept:C0679622
,
umls-concept:C1420219
pubmed:issue
18
pubmed:dateCreated
2008-4-29
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Creatine
,
http://linkedlifedata.com/resource/pubmed/chemical/Glycine
,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Plasma Membrane Neurotransmitter...
,
http://linkedlifedata.com/resource/pubmed/chemical/SLC6A8 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/glycocyamine
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1526-632X
pubmed:author
pubmed-author:AnselmIrina AIA
,
pubmed-author:CoulterDavid LDL
,
pubmed-author:DarrasBasil TBT
pubmed:issnType
Electronic
pubmed:day
29
pubmed:volume
70
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1642-4
pubmed:meshHeading
pubmed-meshheading:18443316-Base Sequence
,
pubmed-meshheading:18443316-Brain Chemistry
,
pubmed-meshheading:18443316-Child
,
pubmed-meshheading:18443316-Child Behavior Disorders
,
pubmed-meshheading:18443316-Creatine
,
pubmed-meshheading:18443316-Developmental Disabilities
,
pubmed-meshheading:18443316-Electrocardiography, Ambulatory
,
pubmed-meshheading:18443316-Exons
,
pubmed-meshheading:18443316-Frameshift Mutation
,
pubmed-meshheading:18443316-Glycine
,
pubmed-meshheading:18443316-Humans
,
pubmed-meshheading:18443316-Language Development Disorders
,
pubmed-meshheading:18443316-Magnetic Resonance Spectroscopy
,
pubmed-meshheading:18443316-Male
,
pubmed-meshheading:18443316-Mental Retardation, X-Linked
,
pubmed-meshheading:18443316-Molecular Sequence Data
,
pubmed-meshheading:18443316-Nerve Tissue Proteins
,
pubmed-meshheading:18443316-Phenotype
,
pubmed-meshheading:18443316-Plasma Membrane Neurotransmitter Transport Proteins
,
pubmed-meshheading:18443316-Sequence Deletion
,
pubmed-meshheading:18443316-Ventricular Premature Complexes
pubmed:year
2008
pubmed:articleTitle
Cardiac manifestations in a child with a novel mutation in creatine transporter gene SLC6A8.
pubmed:affiliation
Department of Neurology, Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA.
pubmed:publicationType
Journal Article
,
Case Reports