@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g
> .
@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:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_head
{
this:
np:hasAssertion
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_assertion
;
np:hasProvenance
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_assertion
a
np:Assertion
.
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_provenance
a
np:Provenance
.
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_assertion
{
miriam-gene:1917
a
ncit:C16612
.
lld:C0342879
a
ncit:C7057
.
dgn-gda:DGNb89fa83977c0f4482ecc2c1af307188d
sio:SIO_000628
miriam-gene:1917
,
lld:C0342879
;
a
sio:SIO_001121
.
}
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_provenance
{
dgn-np:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_assertion
dcterms:description
"[In patients with primary hypercholesterolemia, 23 studies have examined the effects of genetic polymorphisms at 20 different loci on the lipid response to statin treatment, and 18 studies examined genetic polymorphisms involved in the benefits of statin therapy in the prevention of cardiovascular disease.]. 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:15811254
;
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:NP673041.RAA54hgiuGA0vsqoF_0nJE5JmZHSekBUDvjQgVbhEIU_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}