@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA
> .
@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:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_head
{
this:
np:hasAssertion
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_assertion
;
np:hasProvenance
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_provenance
;
np:hasPublicationInfo
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_assertion
a
np:Assertion
.
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_provenance
a
np:Provenance
.
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C0577631
a
ncit:C7057
.
dgn-gda:DGNc80b2cb17cd56bcba151e04de1c0e849
sio:SIO_000628
miriam-gene:1071
,
lld:C0577631
;
a
sio:SIO_001121
.
}
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_provenance
{
dgn-np:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_assertion
dcterms:description
"[CETP and LIPC polymorphisms influence the respective hepatic transcript levels, demonstrate interactions on HDL cholesterol and suggest that imbalances between CETP and LIPC activities may modulate the risk of carotid atherosclerosis.]. 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:21371711
;
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:NP289951.RAoNwwawU2siLcIt0WHUMtNz5Q5OImVL22NMfqyqBNSLA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}