@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y
> .
@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 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:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_head
{
this:
np:hasAssertion
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion
;
np:hasProvenance
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion
a
np:Assertion
.
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_provenance
a
np:Provenance
.
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion
{
miriam-gene:1815
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGN2ff9b8f60b7df2c8a694ae994ceb99f7
sio:SIO_000628
miriam-gene:1815
,
lld:C0005586
;
a
sio:SIO_001122
.
}
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_provenance
{
dgn-np:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_assertion
dct:description
"[ The results suggests that the studied gene variants of type D2 dopamine receptors are not promising candidate genes for bipolar affective illness. We did not consider the family history of the examined subjects, and also the control group was not psychiatrically screened, which may contribute to the lack of significant results.]. 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:15917720
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP45303.RAmSUVPDUZqTKwSmR5ZZOWlvShaCgSekmHmx3panfsm9Y130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}