@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk
> .
@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:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_head
{
this:
np:hasAssertion
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_assertion
;
np:hasProvenance
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_provenance
;
np:hasPublicationInfo
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_assertion
a
np:Assertion
.
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_provenance
a
np:Provenance
.
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN600502c0fd60fd2d69db07efc23eb662
sio:SIO_000628
miriam-gene:1071
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_provenance
{
dgn-np:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_assertion
dcterms:description
"[ In conclusion, the B1B1/CC carriers of the CETP polymorphisms have a more atherogenic lipid profile, including low HDL, and they respond better to statin therapy. These results favor the hypothesis that CETP polymorphisms modify the effect of statin treatment and may help to identify patients who will benefit most from statin therapy.]. 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:12663600
;
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:NP46953.RAGif4q3QvtbFd8sKWoow_Xkau5F393A4o2V6x5e5IJRk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}