@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q
> .
@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:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_head
{
this:
np:hasAssertion
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_assertion
;
np:hasProvenance
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_assertion
a
np:Assertion
.
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_provenance
a
np:Provenance
.
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_assertion
{
miriam-gene:3356
a
ncit:C16612
.
lld:C0686347
a
ncit:C7057
.
dgn-gda:DGN5bbb716c9b10610820b5f34f3f1833d4
sio:SIO_000628
miriam-gene:3356
,
lld:C0686347
;
a
sio:SIO_001121
.
}
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_provenance
{
dgn-np:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_assertion
dcterms:description
"[Abnormalities in dopaminergic activity in the nigrostriatal system have been most often suggested to be involved because the agents which cause TD share in common potent antagonism of dopamine D2 receptors (DRD2), that notably is not balanced by effects such as more potent serotonin (5-HT)2A antagonism.]. 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:16959057
;
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:NP580619.RA2khZILt-hWFUTn9mhGfecLYYrVc-kIcvOeZa0_VAR9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
}