@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw
> .
@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:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_assertion
a
np:Assertion
.
dgn-np:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_provenance
a
np:Provenance
.
dgn-np:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_assertion
{
miriam-gene:291
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN6b1178149fee25ab18876eafd6c69180
sio:SIO_000628
miriam-gene:291
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_provenance
{
dgn-np:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_assertion
dcterms:description
"[To examine whether this genetic variation might contribute to differences in brain activation within the anterior cingulate cortex, we genotyped 16 subjects for the DRD4 and MAOA genes who had been scanned during the ANT.]. 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:12773616
;
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 .
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dgn-np:NP491348.RAHTsN9MyVgZEhJImZmKnCproe26hRLGDkUdeyw45Kluw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
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"v2.1.0" .
}