@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg
> .
@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 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:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_head
{
this:
np:hasAssertion
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_assertion
;
np:hasProvenance
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_provenance
;
np:hasPublicationInfo
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_assertion
a
np:Assertion
.
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_provenance
a
np:Provenance
.
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN92b001d1252c5819583bee1dc7ac84b4
sio:SIO_000628
miriam-gene:3949
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_provenance
{
dgn-np:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_assertion
dct:description
"[Our purpose was to evaluate associations of single nucleotide polymorphisms (SNPs) at the low density lipoprotein (LDL) receptor (LDLR C44857T, minor allele frequency (MAF) 0.26, and A44964G, MAF 0.25, both in the untranslated region) and HMG-CoA reductase (HMGCR i18 T>G, MAF 0.019) gene loci with baseline lipid values, statin-induced LDL-cholesterol (C) lowering response, and incident coronary heart disease (CHD) and cardiovascular disease (CVD) 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:18261733
;
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:NP70915.RAWf6i3Qiww58Y2Gt6tcXW-10kyVLy7CpZnrZjrJfgRjg130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}