@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI
> .
@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:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_head
{
this:
np:hasAssertion
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_assertion
;
np:hasProvenance
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_provenance
;
np:hasPublicationInfo
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_assertion
a
np:Assertion
.
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_provenance
a
np:Provenance
.
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0011581
a
ncit:C7057
.
dgn-gda:DGN8ad0cf54b1ca1b0f5d582cd5bad736a2
sio:SIO_000628
miriam-gene:1813
,
lld:C0011581
;
a
sio:SIO_001121
.
}
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_provenance
{
dgn-np:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_assertion
dcterms:description
"[A number of studies suggest that variants in dopamine receptor genes, such as DRD2, are associated with depression but it is unclear if such variants also modify the association between life events and depression.]. 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:17585060
;
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:NP689472.RAsJlh_t9NCBFA2-97PHKOzuCzsF99bTEWtAsOVEJnAEI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}