@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU
> .
@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:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_head
{
this:
np:hasAssertion
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_assertion
;
np:hasProvenance
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_provenance
;
np:hasPublicationInfo
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_assertion
a
np:Assertion
.
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_provenance
a
np:Provenance
.
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_assertion
{
miriam-gene:7466
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGN65b50fd1bcce3bda6174ab8b380306a4
sio:SIO_000628
miriam-gene:7466
,
lld:C0525045
;
a
sio:SIO_001121
.
}
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_provenance
{
dgn-np:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_assertion
dcterms:description
"[Wolframin gene polymorphisms, including the H611R polymorphism, are reportedly associated with mood disorders and psychiatric hospitalization, but there is disagreement about the association of this specific variant with suicidality and impulsive traits.]. 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:19328217
;
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:NP601476.RAQARmW-wmSXg9loLlWKWzWyM_H9RIYYxBxV8s97EEiSU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}