@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk
> .
@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:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_head
{
this:
np:hasAssertion
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_assertion
;
np:hasProvenance
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_provenance
;
np:hasPublicationInfo
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_assertion
a
np:Assertion
.
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_provenance
a
np:Provenance
.
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0004943
a
ncit:C7057
.
dgn-gda:DGN8a03c6ffab8e1f885e2332a0ef9826e1
sio:SIO_000628
miriam-gene:4846
,
lld:C0004943
;
a
sio:SIO_001121
.
}
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_provenance
{
dgn-np:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_assertion
dcterms:description
"[To assess potential associations between Korean Behçet'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: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:NP228782.RA0F30OCFxAR8T8KMY4v2otbzPTb_akF_dXKtl16OwOTk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}