@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc
> .
@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:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_head
{
this:
np:hasAssertion
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_assertion
;
np:hasProvenance
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_provenance
;
np:hasPublicationInfo
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_assertion
a
np:Assertion
.
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_provenance
a
np:Provenance
.
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0024115
a
ncit:C7057
.
dgn-gda:DGN43c52d564d02591516158e186e501a0a
sio:SIO_000628
miriam-gene:7422
,
lld:C0024115
;
a
sio:SIO_001121
.
}
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_provenance
{
dgn-np:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_assertion
dcterms:description
"[The lack of VEGF in some disease entities may provide implications for its substitution, whereas its overexpression in other lung disorders has led to interventions for the attenuation of its action.]. 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:17044926
;
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:NP571664.RAuGaUgzWDN8ldyMwk6JGZbLvP9hQzqBNwkYxojbsHSFc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}