@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0
> .
@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:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_head
{
this:
np:hasAssertion
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_assertion
;
np:hasProvenance
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_provenance
;
np:hasPublicationInfo
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_assertion
a
np:Assertion
.
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_provenance
a
np:Provenance
.
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_assertion
{
miriam-gene:5104
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNb9233f976af912780af1becd85dd2011
sio:SIO_000628
miriam-gene:5104
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_provenance
{
dgn-np:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_assertion
dcterms:description
"[The results of the present study indicate that the EPHX2 K55R polymorphism is not associated with restenosis after PCI, with incidence of CHD, or with an increased risk of hypertension and therefore, can not serve as a predictor for risk of CHD or restenosis after PCI.]. 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:19814804
;
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:NP417814.RA7RnT6CEENiwyGJGEkw0JVyDVfFR9QTtdSpfyJ4ZDbw0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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" .
}