@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk
> .
@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:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_head
{
this:
np:hasAssertion
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_assertion
;
np:hasProvenance
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_provenance
;
np:hasPublicationInfo
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_assertion
a
np:Assertion
.
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_provenance
a
np:Provenance
.
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0011875
a
ncit:C7057
.
dgn-gda:DGN6c1712bb3ae3bee3aabcdf4a8f091342
sio:SIO_000628
miriam-gene:4846
,
lld:C0011875
;
a
sio:SIO_001121
.
}
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_provenance
{
dgn-np:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_assertion
dcterms:description
"[There are controversial results and insufficient knowledge in the literature about the genetics of diabetes mellitus complications in the Turkish population and endothelial nitric oxide synthase (eNOS) gene polymorphisms may act as a potential modifier of diabetic vascular complications.]. 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:20642368
;
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:NP616628.RABE839cXqRxy0RqPAWqIysV0imr8MfVv6Vpu7FRR52bk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}