@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs
> .
@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:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_head
{
this:
np:hasAssertion
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_assertion
;
np:hasProvenance
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_provenance
;
np:hasPublicationInfo
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_assertion
a
np:Assertion
.
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_provenance
a
np:Provenance
.
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0004943
a
ncit:C7057
.
dgn-gda:DGN452d2236759574d06daaec72dea0c401
sio:SIO_000628
miriam-gene:4846
,
lld:C0004943
;
a
sio:SIO_001122
.
}
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_provenance
{
dgn-np:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_assertion
dcterms:description
"[To assess potential associations between Korean Behet's disease (BD) or other rheumatic diseases with vasculitis and two polymorphisms of the endothelial nitric oxide synthase (eNOS) gene, which include the Glu298Asp polymorphism in exon 7 and a variable number of tandem repeats (VNTR) polymorphism in intron 4.]. 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:14583572
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP61654.RAU3A6CfKppMgCqDhkhUPMYPzzw-Ll0cuEJ3jpl881Jrs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}