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http://rdf.disgenet.org/nanopublications.trig#NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E
> .
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> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
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http://identifiers.org/ncbigene/
> .
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http://identifiers.org/pubmed/
> .
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> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
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> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
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.
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a
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{
dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_assertion
dcterms:description
"[We discovered that variants previously shown to associate with atrial fibrillation (AF), rs2200733 and rs10033464, significantly associated with IS, with the strongest risk for CES. The association with noncardiogenic stroke is intriguing and suggests that atrial fibrillation may be underdiagnosed in patients presenting with stroke. This discovery may have implications for workup and treatment of IS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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pav:importedOn
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xsd:date
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rdfs:comment
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rdfs:label
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{
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xsd:dateTime
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