@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_head
{
this:
np:hasAssertion
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion
;
np:hasProvenance
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance
;
np:hasPublicationInfo
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion
a
np:Assertion
.
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance
a
np:Provenance
.
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN69629d7600d51ec9a34a55840399987d
sio:SIO_000628
miriam-gene:7422
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_provenance
{
dgn-np:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_assertion
dcterms:description
"[Variation in the VEGF gene is weakly associated with IMT and the risk of AMI, but the effect can only be observed when the information of the SNPs is combined by constructing haplotypes.]. 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:19089753
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP119809.RA5ZbEnWAFaG42aO7iLwds_aehkb06qsG06ksY7AvdgNc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:47+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}