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13678589
Source:
http://linkedlifedata.com/resource/pubmed/id/13678589
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0024501
,
umls-concept:C0376315
,
umls-concept:C0721534
,
umls-concept:C1167122
,
umls-concept:C1257825
,
umls-concept:C1514873
,
umls-concept:C1523987
,
umls-concept:C1546857
,
umls-concept:C1556066
,
umls-concept:C1619636
,
umls-concept:C1708025
pubmed:issue
18
pubmed:dateCreated
2003-9-18
pubmed:abstractText
Genome instability is a hallmark of cancer and plays a critical role in generating the myriad of phenotypes selected for during tumor progression. However, the mechanisms that prevent genome rearrangements remain poorly understood.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9107782
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Elg1 protein, S cerevisiae
,
http://linkedlifedata.com/resource/pubmed/chemical/Macromolecular Substances
,
http://linkedlifedata.com/resource/pubmed/chemical/Proliferating Cell Nuclear Antigen
,
http://linkedlifedata.com/resource/pubmed/chemical/RFC1 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Replication Protein C
,
http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0960-9822
pubmed:author
pubmed-author:AgyeiRogerR
,
pubmed-author:DurocherDanielD
,
pubmed-author:KanellisPamelaP
pubmed:issnType
Print
pubmed:day
16
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1583-95
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:13678589-Amino Acid Sequence
,
pubmed-meshheading:13678589-Carrier Proteins
,
pubmed-meshheading:13678589-DNA Damage
,
pubmed-meshheading:13678589-DNA Replication
,
pubmed-meshheading:13678589-DNA-Binding Proteins
,
pubmed-meshheading:13678589-Genome
,
pubmed-meshheading:13678589-Genomic Instability
,
pubmed-meshheading:13678589-Humans
,
pubmed-meshheading:13678589-Macromolecular Substances
,
pubmed-meshheading:13678589-Molecular Sequence Data
,
pubmed-meshheading:13678589-Phylogeny
,
pubmed-meshheading:13678589-Proliferating Cell Nuclear Antigen
,
pubmed-meshheading:13678589-Protein Binding
,
pubmed-meshheading:13678589-Replication Protein C
,
pubmed-meshheading:13678589-Saccharomyces cerevisiae
,
pubmed-meshheading:13678589-Saccharomyces cerevisiae Proteins
,
pubmed-meshheading:13678589-Sequence Alignment
,
pubmed-meshheading:13678589-Transcription Factors
pubmed:year
2003
pubmed:articleTitle
Elg1 forms an alternative PCNA-interacting RFC complex required to maintain genome stability.
pubmed:affiliation
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto, Ontario M5G 1X5, Canada.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't