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12843324
Source:
http://linkedlifedata.com/resource/pubmed/id/12843324
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57
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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:C0008633
,
umls-concept:C0024779
,
umls-concept:C0039082
,
umls-concept:C0079429
,
umls-concept:C1708726
pubmed:issue
7
pubmed:dateCreated
2003-7-4
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/OMIM/113650
,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/601653
,
http://linkedlifedata.com/resource/pubmed/xref/OMIM/602588
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1468-6244
pubmed:author
pubmed-author:BerkmanJJ
,
pubmed-author:GattasMM
,
pubmed-author:GlassII
,
pubmed-author:HenniesH CHC
,
pubmed-author:HildebrandtFF
,
pubmed-author:HylandVV
,
pubmed-author:KrombergJJ
,
pubmed-author:LUEY MYM
,
pubmed-author:LuckeBB
,
pubmed-author:MacmillanJJ
,
pubmed-author:NurnbergGG
,
pubmed-author:NurnbergPP
,
pubmed-author:OttoEE
,
pubmed-author:RufE-MEM
,
pubmed-author:WolfM T FMT
pubmed:issnType
Electronic
pubmed:volume
40
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
515-9
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:12843324-Branchio-Oto-Renal Syndrome
,
pubmed-meshheading:12843324-Chromosome Mapping
,
pubmed-meshheading:12843324-Chromosomes, Human, Pair 14
,
pubmed-meshheading:12843324-DNA
,
pubmed-meshheading:12843324-Family Health
,
pubmed-meshheading:12843324-Female
,
pubmed-meshheading:12843324-Genetic Predisposition to Disease
,
pubmed-meshheading:12843324-Genome, Human
,
pubmed-meshheading:12843324-Haplotypes
,
pubmed-meshheading:12843324-Humans
,
pubmed-meshheading:12843324-Lod Score
,
pubmed-meshheading:12843324-Male
,
pubmed-meshheading:12843324-Microsatellite Repeats
,
pubmed-meshheading:12843324-Pedigree
pubmed:year
2003
pubmed:articleTitle
A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3.
pubmed:publicationType
Letter
,
Research Support, Non-U.S. Gov't