@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_assertion
;
np:hasProvenance
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_provenance
;
np:hasPublicationInfo
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_assertion
a
np:Assertion
.
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_provenance
a
np:Provenance
.
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN0112d0747a3e7232f96a116f51219ab5
sio:SIO_000628
miriam-gene:1813
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_provenance
{
dgn-np:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_assertion
dcterms:description
"[We investigated 16 polymorphisms from three genes, dopamine receptor D2 (DRD2), catechol-O-methyl transferase (COMT) and brain derived neurotrophic factor (BDNF), which are involved in the dopaminergic pathways, and have been reported to be associated with susceptibility to schizophrenia and response to antipsychotic therapy.]. 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:19207030
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP45417.RAVfrmyhh4Zm1H1t-3DEEhqlKpMvGHRcUR-orxVmSj0Lw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}