@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1212398.RAQR8B6_ipTmVOaZII6gIpq-vuWIixfRYNUObYRVy53Ts
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1212398.RAQR8B6_ipTmVOaZII6gIpq-vuWIixfRYNUObYRVy53Ts130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP1212398.RAQR8B6_ipTmVOaZII6gIpq-vuWIixfRYNUObYRVy53Ts130_provenance
a
np:Provenance
.
dgn-np:NP1212398.RAQR8B6_ipTmVOaZII6gIpq-vuWIixfRYNUObYRVy53Ts130_publicationInfo
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{
miriam-gene:58191
a
ncit:C16612
.
lld:C0003850
a
ncit:C7057
.
dgn-gda:DGNf19ddd61e192a09486c490b6f32344b1
sio:SIO_000628
miriam-gene:58191
,
lld:C0003850
;
a
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.
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dgn-np:NP1212398.RAQR8B6_ipTmVOaZII6gIpq-vuWIixfRYNUObYRVy53Ts130_provenance
{
dgn-np:NP1212398.RAQR8B6_ipTmVOaZII6gIpq-vuWIixfRYNUObYRVy53Ts130_assertion
dcterms:description
"[The aim of this study was to analyze the association between I123T and A181V polymorphism haplotypes and the accumulation of carotid plaque as well as the effect of the haplotype on the CXCL16 mRNA expression in carotid plaques in patients with advanced atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
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sio:SIO_000772
miriam-pubmed:25142184
;
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prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1212398.RAQR8B6_ipTmVOaZII6gIpq-vuWIixfRYNUObYRVy53Ts130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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"v4.0.0" .
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