@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k
> .
@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:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_head
{
this:
np:hasAssertion
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_assertion
;
np:hasProvenance
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_assertion
a
np:Assertion
.
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_provenance
a
np:Provenance
.
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_assertion
{
miriam-gene:6531
a
ncit:C16612
.
lld:C0152115
a
ncit:C7057
.
dgn-gda:DGN61486122be697454bb4426f021cd153b
sio:SIO_000628
miriam-gene:6531
,
lld:C0152115
;
a
sio:SIO_001121
.
}
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_provenance
{
dgn-np:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_assertion
dcterms:description
"[We examined three polymorphisms in the dopamine D2 receptor gene (DRD2), two sites in the 3' region of the dopamine transporter (DAT) gene, two sites in the promoter and coding region of the dopamine D4 (DRD4) receptor gene, as well as polymorphic sites in the serotonin 6 receptor gene, the serotonin transporter gene and the tryptophan hydroxylase gene, for association with TD susceptibility.]. 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:14583797
;
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:NP365751.RALlW1pW41AEaTIlO3f6b3AMWKtg4TAmI9ZdhhZ_nRC9k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:34+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" .
}