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12161600
Source:
http://linkedlifedata.com/resource/pubmed/id/12161600
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53
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0028630
,
umls-concept:C0086582
,
umls-concept:C0392747
,
umls-concept:C1136169
,
umls-concept:C1417098
pubmed:issue
8
pubmed:dateCreated
2002-8-5
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Chromosomal Proteins, Non-Histone
,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/MECP2 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Methyl-CpG-Binding Protein 2
,
http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1468-6244
pubmed:author
pubmed-author:HanefeldFF
,
pubmed-author:HuppkePP
,
pubmed-author:LacconeFF
,
pubmed-author:PepinskiWW
,
pubmed-author:TrappeRR
,
pubmed-author:ZollBB
pubmed:issnType
Electronic
pubmed:volume
39
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
586-8
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:12161600-Amino Acid Substitution
,
pubmed-meshheading:12161600-Brain Diseases, Metabolic, Inborn
,
pubmed-meshheading:12161600-Chromosomal Proteins, Non-Histone
,
pubmed-meshheading:12161600-CpG Islands
,
pubmed-meshheading:12161600-DNA-Binding Proteins
,
pubmed-meshheading:12161600-Developmental Disabilities
,
pubmed-meshheading:12161600-Female
,
pubmed-meshheading:12161600-Genetic Testing
,
pubmed-meshheading:12161600-Genetic Variation
,
pubmed-meshheading:12161600-Humans
,
pubmed-meshheading:12161600-Infant
,
pubmed-meshheading:12161600-Intellectual Disability
,
pubmed-meshheading:12161600-Male
,
pubmed-meshheading:12161600-Methyl-CpG-Binding Protein 2
,
pubmed-meshheading:12161600-Microcephaly
,
pubmed-meshheading:12161600-Pedigree
,
pubmed-meshheading:12161600-Point Mutation
,
pubmed-meshheading:12161600-Repressor Proteins
,
pubmed-meshheading:12161600-Rett Syndrome
pubmed:year
2002
pubmed:articleTitle
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution.
pubmed:publicationType
Letter