@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY
> .
@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:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_head
{
this:
np:hasAssertion
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_assertion
;
np:hasProvenance
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_provenance
;
np:hasPublicationInfo
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_assertion
a
np:Assertion
.
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_provenance
a
np:Provenance
.
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0154828
a
ncit:C7057
.
dgn-gda:DGN6cffe0491ae817ab309ffa760323a42b
sio:SIO_000628
miriam-gene:7422
,
lld:C0154828
;
a
sio:SIO_001121
.
}
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_provenance
{
dgn-np:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_assertion
dcterms:description
"[These data demonstrate that regardless of developmental stage of the vascular bed, increased expression of VEGF in the retina is sufficient to cause neovascularization, and high levels of expression cause severe neovascularization and traction retinal detachment.]. 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:11839592
;
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:NP841915.RAKGXJJNEqoNIs5yybqmcp_Shr2uQ6xnYiFt13EocVPLY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:34+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" .
}