@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0
> .
@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:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_head
{
this:
np:hasAssertion
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_assertion
;
np:hasProvenance
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_provenance
;
np:hasPublicationInfo
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_assertion
a
np:Assertion
.
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_provenance
a
np:Provenance
.
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0151313
a
ncit:C7057
.
dgn-gda:DGNc47f9b8a09f1ed8fbf7f46fc287a19f3
sio:SIO_000628
miriam-gene:7422
,
lld:C0151313
;
a
sio:SIO_001121
.
}
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_provenance
{
dgn-np:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_assertion
dcterms:description
"[Preliminary clinical studies have demonstrated improvement in signs and symptoms of sensory neuropathy in patients with lower extremity vascular occlusive disease following intramuscular injection of naked DNA encoding vascular endothelial growth factor (VEGF).]. 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:11529248
;
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:NP369017.RAZjNwKYavpuR7IlkbHnR1uIZhGH5bbB7nHIyanI7KMA0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:36+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" .
}