@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag
> .
@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:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion
;
np:hasProvenance
dgn-np:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance
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np:hasPublicationInfo
dgn-np:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion
a
np:Assertion
.
dgn-np:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance
a
np:Provenance
.
dgn-np:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0020725
a
ncit:C7057
.
dgn-gda:DGNc5edec00ba676b23de0d97f241eb62d0
sio:SIO_000628
miriam-gene:6532
,
lld:C0020725
;
a
sio:SIO_001121
.
}
dgn-np:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_provenance
{
dgn-np:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_assertion
dcterms:description
"[Recent genetic studies have investigated associations between ICD and polymorphisms of genes involved in the dopamine metabolism pathway (COMT, DAT), dopamine receptors (DRD1, DRD2, DRD3, DRD4), serotonin receptors and its transporter (HTR2A, 5HTT), and glutamate receptors (GRIN2B).]. 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:23232665
;
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:NP645943.RAMJpg-0jOr1yVsRJSWt6ePWgzHAesbG5SWU3N9OczVag130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:29+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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}