@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk
> .
@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:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_head
{
this:
np:hasAssertion
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_assertion
;
np:hasProvenance
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_provenance
;
np:hasPublicationInfo
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_assertion
a
np:Assertion
.
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_provenance
a
np:Provenance
.
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_assertion
{
miriam-gene:25890
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGN4826a293fbadc5a89a674b95e4e6ff2e
sio:SIO_000628
miriam-gene:25890
,
lld:C0525045
;
a
sio:SIO_001122
.
}
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_provenance
{
dgn-np:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_assertion
dcterms:description
"[The results suggest that inherited risk for suicide among mood disorder patients is unlikely to be the result of individual common variants of large effect. They nonetheless provide suggestive evidence for multiple loci, which merit further investigation.]. 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:21041247
;
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:NP90501.RA0p46kpY6zVxlMrV6NLAHgWjsHCiLPtBPRO5nBKurDvk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}