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8528262
Source:
http://linkedlifedata.com/resource/pubmed/id/8528262
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55
)
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0017347
,
umls-concept:C0030705
,
umls-concept:C0205082
,
umls-concept:C0206530
,
umls-concept:C0266484
,
umls-concept:C1414394
pubmed:issue
1
pubmed:dateCreated
1996-2-1
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9216904
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers
,
http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
,
http://linkedlifedata.com/resource/pubmed/chemical/empty spiracles homeobox proteins
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1061-4036
pubmed:author
pubmed-author:BoncinelliEE
,
pubmed-author:BrunelliSS
,
pubmed-author:CamaAA
,
pubmed-author:CapraVV
,
pubmed-author:FaiellaAA
,
pubmed-author:NigroVV
,
pubmed-author:SimeoniEE
pubmed:issnType
Print
pubmed:volume
12
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
94-6
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8528262-Base Sequence
,
pubmed-meshheading:8528262-Brain
,
pubmed-meshheading:8528262-Brain Diseases
,
pubmed-meshheading:8528262-DNA Primers
,
pubmed-meshheading:8528262-Female
,
pubmed-meshheading:8528262-Genes, Homeobox
,
pubmed-meshheading:8528262-Homeodomain Proteins
,
pubmed-meshheading:8528262-Humans
,
pubmed-meshheading:8528262-Magnetic Resonance Imaging
,
pubmed-meshheading:8528262-Male
,
pubmed-meshheading:8528262-Molecular Sequence Data
,
pubmed-meshheading:8528262-Nerve Tissue Proteins
,
pubmed-meshheading:8528262-Pedigree
,
pubmed-meshheading:8528262-Point Mutation
,
pubmed-meshheading:8528262-Polymorphism, Single-Stranded Conformational
,
pubmed-meshheading:8528262-Tomography, X-Ray Computed
,
pubmed-meshheading:8528262-Transcription Factors
pubmed:year
1996
pubmed:articleTitle
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.
pubmed:affiliation
DIBIT, Istituto Scientifico HS Raffaele, Milan, Italy.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't