@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE
> .
@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:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_head
{
this:
np:hasAssertion
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_assertion
;
np:hasProvenance
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_provenance
;
np:hasPublicationInfo
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_assertion
a
np:Assertion
.
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_provenance
a
np:Provenance
.
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0021051
a
ncit:C7057
.
dgn-gda:DGN9ebae1bf8c7a3383a5d0d0d6e71e64de
sio:SIO_000628
miriam-gene:7422
,
lld:C0021051
;
a
sio:SIO_001121
.
}
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_provenance
{
dgn-np:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_assertion
dcterms:description
"[We introduced an antisense VEGF expression construct into glioblastoma cells and found that (i) VEGF mRNA and protein levels were markedly reduced, (ii) the modified cells did not secrete sufficient factors so as to be chemoattractive for primary human microvascular endothelial cells, (iii) the modified cells were not able to sustain tumor growth in immunodeficient animals, and (iv) the density of in vivo blood vessel formation was reduced in direct relation to the reduction of VEGF secretion and tumor formation.]. 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:8710899
;
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:NP661999.RAcXm5DP1J8YNi9ZlG8dhSrQ61OIfju31j9XWKh8bXIzE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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" .
}