@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM
> .
@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:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_head
{
this:
np:hasAssertion
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_assertion
;
np:hasProvenance
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_provenance
;
np:hasPublicationInfo
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_assertion
a
np:Assertion
.
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_provenance
a
np:Provenance
.
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_assertion
{
miriam-gene:6571
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNa769df0fb91d1887e2a6a6e0401ffc41
sio:SIO_000628
miriam-gene:6571
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_provenance
{
dgn-np:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_assertion
dcterms:description
"[Examination of VMAT2 variants can provide potential insights into roles for allelic variants at these loci in variant drug responses and in diseases linked to monoaminergic systems, including substance abuse and Parkinson's disease.]. 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:11099463
;
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:NP249819.RA_xOjxtVTetiKeBSWaSsWfBFVas2_sm5WrrJUc-DFRAM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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
<
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> , <
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" .
}