@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA
> .
@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:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_head
{
this:
np:hasAssertion
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_assertion
;
np:hasProvenance
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_provenance
;
np:hasPublicationInfo
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_assertion
a
np:Assertion
.
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_provenance
a
np:Provenance
.
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_assertion
{
miriam-gene:56117
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGNb252211e3929bf0d1a31a086e67a6138
sio:SIO_000628
miriam-gene:56117
,
lld:C0525045
;
a
sio:SIO_001121
.
}
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_provenance
{
dgn-np:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_assertion
dcterms:description
"[The results showed that the triplet repeat polymorphism in the promoter region of the CNR1 gene was not likely to be involved in the pathogenesis or in the psychotic symptoms of mood disorders.]. 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:11353438
;
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:NP267816.RAfPbutZuH2NoU65VDs0J-dolriULYlNstPASViA3MVCA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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
<
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" .
}