@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE
> .
@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:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_head
{
this:
np:hasAssertion
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_assertion
;
np:hasProvenance
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_provenance
;
np:hasPublicationInfo
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_assertion
a
np:Assertion
.
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_provenance
a
np:Provenance
.
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C1863535
a
ncit:C7057
.
dgn-gda:DGN9fb6d1839198eb2e89d2baefc4d84e2f
sio:SIO_000628
miriam-gene:1813
,
lld:C1863535
;
a
sio:SIO_001121
.
}
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_provenance
{
dgn-np:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_assertion
dcterms:description
"[The dopamine D2 receptor gene (DRD2) was chosen as a candidate gene for general cognitive ability (g) since it has been found to be associated with visuospatial ability which in turn is highly correlated with g. Confirming two similar studies in children, however, no significant differences were obtained.]. 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:11261743
;
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:NP813155.RAeZoD_Msn8eEqJXki95RDJ-7Fbm7jPSATDiLy-JmIbKE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}