@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g
> .
@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:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_head
{
this:
np:hasAssertion
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_assertion
;
np:hasProvenance
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_provenance
;
np:hasPublicationInfo
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_assertion
a
np:Assertion
.
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_provenance
a
np:Provenance
.
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0020725
a
ncit:C7057
.
dgn-gda:DGN94091058db0f24a9bcbcc6b6c91e825e
sio:SIO_000628
miriam-gene:1312
,
lld:C0020725
;
a
sio:SIO_001121
.
}
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_provenance
{
dgn-np:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_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:NP916729.RAbDtsETJAZA8B-bLHQx2C9vZTFCJIJ6olmY1HgyWRg6g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}