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15880745
Source:
http://linkedlifedata.com/resource/pubmed/id/15880745
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64
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0205242
,
umls-concept:C0231024
,
umls-concept:C0243067
,
umls-concept:C0919427
,
umls-concept:C1420117
,
umls-concept:C1882417
,
umls-concept:C2603343
,
umls-concept:C2827582
pubmed:issue
2
pubmed:dateCreated
2005-5-26
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/DE 08559
,
http://linkedlifedata.com/resource/pubmed/grant/DE 13076
,
http://linkedlifedata.com/resource/pubmed/grant/ES11375
,
http://linkedlifedata.com/resource/pubmed/grant/NS39818
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Methylenetetrahydrofolate...
,
http://linkedlifedata.com/resource/pubmed/chemical/SLC19A2 protein, human
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1552-4825
pubmed:author
pubmed-author:CastillaEduardo EEE
,
pubmed-author:CooperMargaret EME
,
pubmed-author:Lennon-GrahamFeliciaF
,
pubmed-author:MarazitaMary LML
,
pubmed-author:MurrayJeffrey CJC
,
pubmed-author:OrioliIêda MIM
,
pubmed-author:SpeerMarcyM
,
pubmed-author:TrembathDimitriD
,
pubmed-author:VieiraAlexandre RAR
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
135
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
220-3
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:15880745-Alleles
,
pubmed-meshheading:15880745-Cleft Lip
,
pubmed-meshheading:15880745-Cleft Palate
,
pubmed-meshheading:15880745-Family Health
,
pubmed-meshheading:15880745-Female
,
pubmed-meshheading:15880745-Gene Frequency
,
pubmed-meshheading:15880745-Genotype
,
pubmed-meshheading:15880745-Humans
,
pubmed-meshheading:15880745-Linkage Disequilibrium
,
pubmed-meshheading:15880745-Male
,
pubmed-meshheading:15880745-Membrane Transport Proteins
,
pubmed-meshheading:15880745-Methylenetetrahydrofolate Reductase (NADPH2)
,
pubmed-meshheading:15880745-Neural Tube Defects
,
pubmed-meshheading:15880745-Pedigree
,
pubmed-meshheading:15880745-Point Mutation
,
pubmed-meshheading:15880745-Polymorphism, Genetic
pubmed:year
2005
pubmed:articleTitle
Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects.
pubmed:publicationType
Letter
,
Comparative Study
,
Research Support, U.S. Gov't, P.H.S.
,
Research Support, Non-U.S. Gov't
,
Multicenter Study
,
Research Support, N.I.H., Extramural