@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs
> .
@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:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_head
{
this:
np:hasAssertion
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_assertion
;
np:hasProvenance
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_provenance
;
np:hasPublicationInfo
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_assertion
a
np:Assertion
.
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_provenance
a
np:Provenance
.
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0035320
a
ncit:C7057
.
dgn-gda:DGN375879e8f97753834259791e72fa7001
sio:SIO_000628
miriam-gene:7422
,
lld:C0035320
;
a
sio:SIO_001123
.
}
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_provenance
{
dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_assertion
dcterms:description
"[Vector-based vascular endothelial growth factor 165 (VEGF) (165) targeted siRNA expression system (pSilencer (siVEGF)) was used to investigate the ability to inhibit VEGF (165) expression in vitro and suppresses retinal neovascularization.]. 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:18978955
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:19+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" .
}