@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg
> .
@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:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_head
{
this:
np:hasAssertion
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_assertion
;
np:hasProvenance
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_provenance
;
np:hasPublicationInfo
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_assertion
a
np:Assertion
.
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_provenance
a
np:Provenance
.
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_assertion
{
miriam-gene:6296
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN60b4fdde2dedadd5553ec76c15e86ce7
sio:SIO_000628
miriam-gene:6296
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_provenance
{
dgn-np:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_assertion
dcterms:description
"[Our results showed that endothelial dysfunction induced by intracellular SAH accumulation is mediated by regulating the expression of atherosclerosis related genes in HUVEC, which is not related with gene promoter methylated patterns, but may be associated with altered global DNA hypomethylated status.]. 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:19958400
;
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:NP377588.RAfFKoGA92T6EF-LezEVVSS8XUu5bDaDbCxDurLbiN6gg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:41+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" .
}