@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY
> .
@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:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_head
{
this:
np:hasAssertion
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_assertion
;
np:hasProvenance
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_provenance
;
np:hasPublicationInfo
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_assertion
a
np:Assertion
.
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_provenance
a
np:Provenance
.
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_assertion
{
miriam-gene:5243
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGNd3f4201655bf43a747f491f5ff1c5b5e
sio:SIO_000628
miriam-gene:5243
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_provenance
{
dgn-np:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_assertion
dcterms:description
"[This is the first study to demonstrate that common genetic variability within the SLCO1B1 and ABCB1 genes is associated with the modification of the effectiveness of statins in the prevention of the clinical outcome, myocardial infarction.]. 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:20712525
;
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:NP929120.RArDg7oLk84MuJyY5nXpJDA2QtF5LHoPU8OXzsg5AIjrY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:30+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" .
}