@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8
> .
@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:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_head
{
this:
np:hasAssertion
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_assertion
;
np:hasProvenance
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_provenance
;
np:hasPublicationInfo
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_assertion
a
np:Assertion
.
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_provenance
a
np:Provenance
.
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0520679
a
ncit:C7057
.
dgn-gda:DGNde95259318d547046342d11caba916b7
sio:SIO_000628
miriam-gene:4846
,
lld:C0520679
;
a
sio:SIO_001121
.
}
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_provenance
{
dgn-np:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_assertion
dcterms:description
"[Since expression of the eNOS gene is regulated by epigenetic mechanisms and OSA may cause epigenetic modifications such as DNA hypermethylation, we hypothesized that epigenetic modifications in the eNOS gene may underlie the differential vascular phenotypes in pediatric OSA.]. 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:23328840
;
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:NP632870.RARp8x2c2PT_10wYQbCEXewA9b9muk2Fb7qKAIPKbNOL8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}