@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A
> .
@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:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_head
{
this:
np:hasAssertion
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_assertion
;
np:hasProvenance
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_assertion
a
np:Assertion
.
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_provenance
a
np:Provenance
.
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_assertion
{
miriam-gene:255738
a
ncit:C16612
.
lld:C0242339
a
ncit:C7057
.
dgn-gda:DGN2f1d4146a472cf3b78e3d1f36553057d
sio:SIO_000628
miriam-gene:255738
,
lld:C0242339
;
a
sio:SIO_001121
.
}
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_provenance
{
dgn-np:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_assertion
dcterms:description
"[These results, combined with the significant rise in PCSK9 levels after statin therapy, warrant further studies in order to unravel the exact role of PCSK9 in the pathogenesis and treatment of this highly prevalent genetic dyslipidaemia.]. 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:21539517
;
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:NP771676.RA0cu5v6Eup2652FxSZ8PY-sXt4zJoo2p9af7P6Lf_c8A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}