@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA
> .
@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:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_head
{
this:
np:hasAssertion
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_assertion
;
np:hasProvenance
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_provenance
;
np:hasPublicationInfo
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_assertion
a
np:Assertion
.
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_provenance
a
np:Provenance
.
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_assertion
{
miriam-gene:345
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN1c72fcb86f42463a8ccf046b6726cd1e
sio:SIO_000628
miriam-gene:345
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_provenance
{
dgn-np:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_assertion
dcterms:description
"[While there is no evidence for a significant association of several common lipoprotein-related genetic variants with carotid IMT, 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: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:NP900038.RAecX0iQRpu6V6lIi1lmA4fp1rZqp76VxIYLitQ7uHjwA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:13+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" .
}