@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI
> .
@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:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_head
{
this:
np:hasAssertion
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_assertion
;
np:hasProvenance
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_provenance
;
np:hasPublicationInfo
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_assertion
a
np:Assertion
.
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_provenance
a
np:Provenance
.
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN357ee6eaa4eefb12ccd570e7f8be551a
sio:SIO_000628
miriam-gene:4023
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_provenance
{
dgn-np:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_assertion
dcterms:description
"[our results are consistent with the previously reported role of CETP and LPL genetic variants in cardiovascular risk and the possible modulation of the association between hypertension and carotid IMT by APOCIII Sst-1 variant.]. 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:16430904
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP123249.RAtizK0VEcNpN-L-crai2RQgGavTYzddprOw1jvrfYRQI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:04+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" .
}