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> .
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> .
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http://semanticscience.org/resource/
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> .
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http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
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http://identifiers.org/pubmed/
> .
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> .
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http://purl.org/ontology/wi/core#
> .
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> .
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http://purl.org/pav/
> .
@prefix prv: <
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> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
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{
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np:Assertion
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a
ncit:C16612
.
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a
ncit:C7057
.
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{
dgn-np:NP986179.RA1chB01LGokkaQp_kVxAtb5sdXHD3DORqjz96hwh1o_Q130_assertion
dcterms:description
"[In this work we investigated the following: i) whether CAV1 is a quantitative trait locus of clustering of atherothrombotic traits associated with MS; ii) whether CVA1 is associated with hypertension or MS in hypertensive patients; and iii) whether genetic interaction between NOS3 and CAV1 is involved in the susceptibility or protection to hypertension associated with MS. To carry out the study, we genotyped 285 randomly selected individuals and 175 hypertensive patients, all of them < or = 60 years old, with two polymorphisms of the CAV1 gene: the 22285 C>T and the 22375-22375 del AC (GenBank AF125348), and the 1132T>C polymorphism of the NOS3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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eco:ECO_0000203
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xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP986179.RA1chB01LGokkaQp_kVxAtb5sdXHD3DORqjz96hwh1o_Q130_publicationInfo
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xsd:dateTime
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> , <
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