@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4
> .
@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:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_head
{
this:
np:hasAssertion
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_assertion
;
np:hasProvenance
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_provenance
;
np:hasPublicationInfo
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_assertion
a
np:Assertion
.
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_provenance
a
np:Provenance
.
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_assertion
{
miriam-gene:27185
a
ncit:C16612
.
lld:C0006012
a
ncit:C7057
.
dgn-gda:DGNbae2ee1d1b069ef56bec01d4970e1496
sio:SIO_000628
miriam-gene:27185
,
lld:C0006012
;
a
sio:SIO_001121
.
}
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_provenance
{
dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_assertion
dcterms:description
"[These results support involvement of DISC1 in the genetic aetiology of BPD and suggest that its distinct variants contribute to variation in the dimensional features of psychotic and bipolar spectrum 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:17673452
;
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 .
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dgn-np:NP615163.RAgPWRMC8O99tbOExtnLk5kOO7QulzeNOBCVooKbzFWT4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}