@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s
> .
@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:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_head
{
this:
np:hasAssertion
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_assertion
;
np:hasProvenance
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_provenance
;
np:hasPublicationInfo
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_assertion
a
np:Assertion
.
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_provenance
a
np:Provenance
.
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_assertion
{
miriam-gene:1917
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGN748a83964c7c8e5af0b6b2b572be0846
sio:SIO_000628
miriam-gene:1917
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_provenance
{
dgn-np:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_assertion
dcterms:description
"[Our goal was to determine whether genetic variation at genes affecting statin metabolism or targets of statin therapy would influence low density lipoprotein (LDL) cholesterol lowering with pravastatin, baseline heart disease, or cardiac endpoints on trial.]. 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:22189199
;
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:NP510612.RAPCvMthJ7QVifX0oNXfhYJxSQcbrmSI2f13ShIbLTI3s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}