@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg
> .
@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#
> .
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_head
{
this:
np:hasAssertion
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_assertion
;
np:hasProvenance
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_provenance
;
np:hasPublicationInfo
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_assertion
a
np:Assertion
.
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_provenance
a
np:Provenance
.
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_assertion
{
miriam-gene:7350
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGNbdc1befefd5ce549e0c79ee4581eb363
sio:SIO_000628
miriam-gene:7350
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_provenance
{
dgn-np:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_assertion
dcterms:description
"[Participants from the Utrecht Cardiovascular Pharmacogenetics (UCP) studies were enrolled from a population-based registry of pharmacy records linked to hospital discharge records (PHARMO) to investigate tagging SNPs within candidate genes involved in the cholesterol lowering pathway for modification of the effectiveness of statins in reducing the risk of myocardial infarction (MI).]. 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:21741043
;
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:NP786174.RAkqOWnpcjZy8Ux68AxAo6uA-ZX4ZfkM5c75jgHQfb4Yg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+02:00"^^
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
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}