@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg
> .
@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:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_head
{
this:
np:hasAssertion
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_assertion
;
np:hasProvenance
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_provenance
;
np:hasPublicationInfo
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_assertion
a
np:Assertion
.
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_provenance
a
np:Provenance
.
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_assertion
{
miriam-gene:1815
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN249be773d9a0735d81001e82bab25d6c
sio:SIO_000628
miriam-gene:1815
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_provenance
{
dgn-np:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_assertion
dcterms:description
"[Polymorphisms in the catechol-O-methyltransferase (COMT) and the dopamine D4 receptor (DRD4) genes are likely to impact directly on the functioning of the frontal cortex, whereas polymorphisms in the dopamine D2 receptor (DRD2) and dopamine transporter (DAT1) genes might influence frontal cortex functioning indirectly via strong frontostriatal connections.]. 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:20210499
;
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:NP377112.RAcaPgzN9A9KBU1CjEBfItvk_RdLVef9wwsehJHx8ordg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}