@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA
> .
@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:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_head
{
this:
np:hasAssertion
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_assertion
;
np:hasProvenance
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_provenance
;
np:hasPublicationInfo
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_assertion
a
np:Assertion
.
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_provenance
a
np:Provenance
.
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_assertion
{
miriam-gene:4973
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN2dcfadf5ca4db48fd943a081a04bb444
sio:SIO_000628
miriam-gene:4973
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_provenance
{
dgn-np:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_assertion
dcterms:description
"[In NASH, the LOX-1 polymorphism is associated with liver disease severity and may predispose to CVD through modulation of postprandial small TRLPs and adipokine balance and to diabetes by affecting both insulin secretion and insulin sensitivity.]. 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:21865331
;
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:NP533797.RACxBP8sbAqhLyGOi5LmP65y_QSXEh37808LHaGO4I5vA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}