@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ
> .
@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:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_head
{
this:
np:hasAssertion
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_assertion
;
np:hasProvenance
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_assertion
a
np:Assertion
.
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_provenance
a
np:Provenance
.
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_assertion
{
miriam-gene:4018
a
ncit:C16612
.
lld:C0020443
a
ncit:C7057
.
dgn-gda:DGN0e6497f8dc2cb0afd51abd3d5fd046c4
sio:SIO_000628
miriam-gene:4018
,
lld:C0020443
;
a
sio:SIO_001121
.
}
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_provenance
{
dgn-np:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_assertion
dcterms:description
"[To test the hypothesis that increased plasma levels of Lp(a) may enhance the development of atherosclerosis in the setting of hypercholesterolemia, we generated Watanabe heritable hyperlipidemic (WHHL) transgenic (Tg) rabbits expressing human apolipoprotein(a) (apo(a)).]. 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:12196525
;
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:NP541838.RAhzXqLXIbaCnSxfdr-n79FDLlzSExv_dEmXFYrudp2bQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:27+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" .
}