@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@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#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_assertion
;
np:hasProvenance
dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_provenance
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np:hasPublicationInfo
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;
a
np:Nanopublication
.
dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_assertion
a
np:Assertion
.
dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_provenance
a
np:Provenance
.
dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_assertion
{
miriam-gene:404677
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN02c96e3e8d155767c5e01ac1876a235f
sio:SIO_000628
miriam-gene:404677
,
lld:C0010068
;
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.
}
dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_provenance
{
dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_assertion
dcterms:description
"[We tested the impact of genetic risk score (GRS(24SNP/CAD)) calculated as a weighted (by allelic odds ratios for CAD) sum of CAD risk alleles from the studied 24 variants on CIMT, CAE, the incidence of carotid atherosclerosis and the progression of CIMT and CAE during a 6-year follow-up.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:22295058
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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 .
}
dgn-np:NP270713.RA1w5in3x99Pxtoqh36WGkxNSgAS3L71VsTQ2k0VYSaDk130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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dgn-void:disgenetrdf
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}