@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8
> .
@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:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_head
{
this:
np:hasAssertion
dgn-np:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_assertion
a
np:Assertion
.
dgn-np:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_provenance
a
np:Provenance
.
dgn-np:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_assertion
{
miriam-gene:79789
a
ncit:C16612
.
lld:C0021368
a
ncit:C7057
.
dgn-gda:DGN9e73cdf393533403807995f8fcd3a8fc
sio:SIO_000628
miriam-gene:79789
,
lld:C0021368
;
a
sio:SIO_001122
.
}
dgn-np:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_provenance
{
dgn-np:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_assertion
dcterms:description
"[Using combined GWA analysis from three clinical trials involving nearly 4,000 individuals treated with simvastatin, pravastatin, or atorvastatin, we have identified SNPs that may be associated with variation in the magnitude of statin-mediated reduction in total and LDL-cholesterol, including one in the CLMN gene for which statistical evidence for association exceeds conventional levels of genome-wide significance.]. 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:20339536
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP89979.RAeqgiZzmGMd3MuWnwVsjx2TjbGyhuqhpsP4DytB4YUY8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:44+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
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dgn-void:disgenetrdf
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"v2.1.0" .
}