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10905895
Source:
http://linkedlifedata.com/resource/pubmed/id/10905895
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48
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Inference
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0021149
,
umls-concept:C0026882
,
umls-concept:C0035687
,
umls-concept:C0175694
,
umls-concept:C0441712
,
umls-concept:C0678227
,
umls-concept:C0887918
,
umls-concept:C1521991
pubmed:issue
5
pubmed:dateCreated
2000-7-17
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF132981
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/7-dehydrocholesterol reductase
,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary
,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidoreductases
,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidoreductases Acting on CH-CH...
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1468-6244
pubmed:author
pubmed-author:HennekamR CRC
,
pubmed-author:OostheimWW
,
pubmed-author:RomeijnG JGJ
,
pubmed-author:WandersR JRJ
,
pubmed-author:WaterhamH RHR
pubmed:issnType
Electronic
pubmed:volume
37
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
387-9
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:10905895-Alternative Splicing
,
pubmed-meshheading:10905895-Base Sequence
,
pubmed-meshheading:10905895-DNA, Complementary
,
pubmed-meshheading:10905895-Humans
,
pubmed-meshheading:10905895-Introns
,
pubmed-meshheading:10905895-Molecular Sequence Data
,
pubmed-meshheading:10905895-Oxidoreductases
,
pubmed-meshheading:10905895-Oxidoreductases Acting on CH-CH Group Donors
,
pubmed-meshheading:10905895-Point Mutation
,
pubmed-meshheading:10905895-Reverse Transcriptase Polymerase Chain Reaction
,
pubmed-meshheading:10905895-Sequence Analysis, DNA
,
pubmed-meshheading:10905895-Smith-Lemli-Opitz Syndrome
pubmed:year
2000
pubmed:articleTitle
Incidence and molecular mechanism of aberrant splicing owing to a G-->C splice acceptor site mutation causing Smith-Lemli-Opitz syndrome.
pubmed:publicationType
Letter