@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_head
{
this:
np:hasAssertion
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_assertion
;
np:hasProvenance
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_provenance
;
np:hasPublicationInfo
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_assertion
a
np:Assertion
.
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_provenance
a
np:Provenance
.
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_assertion
{
miriam-gene:2053
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGN67a44352efc22c035770b5ee11cf5b75
sio:SIO_000628
miriam-gene:2053
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_provenance
{
dgn-np:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_assertion
dcterms:description
"[This study tested the hypothesis that variations in the EPHX2 gene encoding human soluble epoxide hydrolase (sEH) are associated with atrial fibrillation (AF) and recurrence of atrial fibrillation after catheter ablation.]. 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:23711456
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP377606.RA_GgmiEoyM_De8UGnUE8t3T2kKeYGinszVgpSC4yfVVE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:18+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}