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9171822
Source:
http://linkedlifedata.com/resource/pubmed/id/9171822
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58
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0010308
,
umls-concept:C0026882
,
umls-concept:C0597484
,
umls-concept:C0598849
,
umls-concept:C1314792
pubmed:issue
2
pubmed:dateCreated
1997-6-18
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/SWISSPROT/P07117
,
http://linkedlifedata.com/resource/pubmed/xref/SWISSPROT/P13866
,
http://linkedlifedata.com/resource/pubmed/xref/SWISSPROT/P16256
,
http://linkedlifedata.com/resource/pubmed/xref/SWISSPROT/P26430
,
http://linkedlifedata.com/resource/pubmed/xref/SWISSPROT/P31636
,
http://linkedlifedata.com/resource/pubmed/xref/SWISSPROT/P53794
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/9171822-9288112
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9216904
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Symporters
,
http://linkedlifedata.com/resource/pubmed/chemical/sodium-iodide symporter
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1061-4036
pubmed:author
pubmed-author:AminoNN
,
pubmed-author:FujiwaraHH
,
pubmed-author:HaradaTT
,
pubmed-author:MikiKK
,
pubmed-author:MiyaiKK
,
pubmed-author:TakaiSS
,
pubmed-author:TatsumiKK
pubmed:issnType
Print
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
124-5
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9171822-Amino Acid Sequence
,
pubmed-meshheading:9171822-Animals
,
pubmed-meshheading:9171822-Carrier Proteins
,
pubmed-meshheading:9171822-Cell Line
,
pubmed-meshheading:9171822-Congenital Hypothyroidism
,
pubmed-meshheading:9171822-Female
,
pubmed-meshheading:9171822-Homozygote
,
pubmed-meshheading:9171822-Humans
,
pubmed-meshheading:9171822-Hypothyroidism
,
pubmed-meshheading:9171822-Membrane Proteins
,
pubmed-meshheading:9171822-Molecular Sequence Data
,
pubmed-meshheading:9171822-Mutation
,
pubmed-meshheading:9171822-Pedigree
,
pubmed-meshheading:9171822-Sequence Homology, Amino Acid
,
pubmed-meshheading:9171822-Symporters
pubmed:year
1997
pubmed:articleTitle
Congenital hypothyroidism caused by a mutation in the Na+/I- symporter.
pubmed:publicationType
Letter
,
Case Reports
,
Research Support, Non-U.S. Gov't