@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0
> .
@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:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_head
{
this:
np:hasAssertion
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_assertion
;
np:hasProvenance
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_provenance
;
np:hasPublicationInfo
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_assertion
a
np:Assertion
.
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_provenance
a
np:Provenance
.
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0948089
a
ncit:C7057
.
dgn-gda:DGN0dcf7dc94b648650e0f61a2fbc298d3f
sio:SIO_000628
miriam-gene:7422
,
lld:C0948089
;
a
sio:SIO_001121
.
}
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_provenance
{
dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_assertion
dcterms:description
"[Several common polymorphisms in the promoter region of the VEGF gene have been reported, but only few single nucleotide polymorphisms (SNPs) have been demonstrated to be associated with variations in VEGF serum concentrations and with a susceptibility to CAD and its complications-acute coronary syndromes.]. 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:20210775
;
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:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:06+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" .
}