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10819641
Source:
http://linkedlifedata.com/resource/pubmed/id/10819641
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57
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0002066
,
umls-concept:C0017337
,
umls-concept:C0018591
,
umls-concept:C0022277
,
umls-concept:C0026882
,
umls-concept:C0062939
,
umls-concept:C0205314
,
umls-concept:C0678257
,
umls-concept:C0679622
,
umls-concept:C1706907
,
umls-concept:C1882417
,
umls-concept:C1979963
,
umls-concept:C2003903
pubmed:issue
4
pubmed:dateCreated
2000-5-16
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Dioxygenases
,
http://linkedlifedata.com/resource/pubmed/chemical/Homogentisate 1,2-Dioxygenase
,
http://linkedlifedata.com/resource/pubmed/chemical/Oxygenases
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0022-2593
pubmed:author
pubmed-author:ChiarelliII
,
pubmed-author:De BernabéD BDB
,
pubmed-author:De CórdobaS RSR
,
pubmed-author:GrazianoCC
,
pubmed-author:MannoniAA
,
pubmed-author:MorroneAA
,
pubmed-author:PorfirioBB
,
pubmed-author:ZammarchiEE
pubmed:issnType
Print
pubmed:volume
37
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
309-12
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:10819641-Adult
,
pubmed-meshheading:10819641-Alkaptonuria
,
pubmed-meshheading:10819641-Dioxygenases
,
pubmed-meshheading:10819641-Genetic Heterogeneity
,
pubmed-meshheading:10819641-Haplotypes
,
pubmed-meshheading:10819641-Homogentisate 1,2-Dioxygenase
,
pubmed-meshheading:10819641-Humans
,
pubmed-meshheading:10819641-Infant, Newborn
,
pubmed-meshheading:10819641-Introns
,
pubmed-meshheading:10819641-Italy
,
pubmed-meshheading:10819641-Mutation, Missense
,
pubmed-meshheading:10819641-Oxygenases
,
pubmed-meshheading:10819641-Polymorphism, Genetic
pubmed:year
2000
pubmed:articleTitle
Alkaptonuria in Italy: polymorphic haplotype background, mutational profile, and description of four novel mutations in the homogentisate 1,2-dioxygenase gene.
pubmed:publicationType
Letter
,
Case Reports
,
Research Support, Non-U.S. Gov't