@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk
> .
@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:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_head
{
this:
np:hasAssertion
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_assertion
;
np:hasProvenance
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_assertion
a
np:Assertion
.
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_provenance
a
np:Provenance
.
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_assertion
{
miriam-gene:3990
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN630ec75aa3d7a9eee5db4340e9c258d1
sio:SIO_000628
miriam-gene:3990
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_provenance
{
dgn-np:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_assertion
dcterms:description
"[In the current study, to elucidate the clinical significance of and atherogenicity in marked HALP, we determined the incidence of atherosclerotic cardiovascular disease (ACD) in patients with marked HALP and characterized the lipoprotein abnormalities in those who had ACD, focusing especially on CETP and HTGL.]. 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:7583564
;
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:NP219780.RA_dZ4Pou36nvP3BiPLDMWEpog5BUp31dnmkI4e5gpzFk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}