@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g
> .
@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:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_head
{
this:
np:hasAssertion
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_assertion
;
np:hasProvenance
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_assertion
a
np:Assertion
.
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_provenance
a
np:Provenance
.
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_assertion
{
miriam-gene:3791
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN0b80409013ccd5077ef54075bf666bd1
sio:SIO_000628
miriam-gene:3791
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_provenance
{
dgn-np:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_assertion
dcterms:description
"[These results indicated that upregulated apelin in type 2 diabetes, which may be attributed to increased fat mass, promotes angiogenesis in glomeruli to form abnormal vessels and that enhanced apelin increases permeability via upregulating the expression of VEGFR2 and Tie2 in glomerular endothelial cells.]. 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:23577111
;
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:NP573185.RA7lVc5sT3RlQoe9715jeXVN288DRncRxebQeY-vLkF_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}