@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc
> .
@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:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_head
{
this:
np:hasAssertion
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_assertion
;
np:hasProvenance
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_provenance
;
np:hasPublicationInfo
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_assertion
a
np:Assertion
.
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_provenance
a
np:Provenance
.
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C2733225
a
ncit:C7057
.
dgn-gda:DGNb12befe7054e15632f8da988b95524a2
sio:SIO_000628
miriam-gene:4023
,
lld:C2733225
;
a
sio:SIO_001121
.
}
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_provenance
{
dgn-np:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_assertion
dcterms:description
"[As enzymes that hydrolyze triglyceride-rich lipoproteins are associated with a modulation of both HDL cholesterol and triglycerides, we have tested the hypothesis that mutations in the genes encoding lipoprotein lipase (LPL) or hepatic lipase (HTGL) may contribute to the formation of coronary atherosclerosis and, thus, of coronary heart disease (CHD).]. 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:10729390
;
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:NP509602.RAcMK24VNPyb4l3Y-hxxTtvWZQncM1j4SoIvYwRrPtzTc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}