@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80
> .
@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 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:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_head
{
this:
np:hasAssertion
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_assertion
;
np:hasProvenance
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_provenance
;
np:hasPublicationInfo
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_assertion
a
np:Assertion
.
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_provenance
a
np:Provenance
.
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_assertion
{
miriam-gene:1267
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNb6c2eacd463807884ffcd1c1ab18369e
sio:SIO_000628
miriam-gene:1267
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_provenance
{
dgn-np:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_assertion
dct:description
"[To obtain independent support for this association, we sought evidence for genetic interaction between OLIG2 and three genes of relevance to oligodendrocyte function for which we have reported evidence for association with schizophrenia: CNP, NRG1, and ERBB4.]. 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:16891421
;
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:NP59843.RAzjrr2X6MShnBWYRyjq9PtH8G9RDEft8CbwAKPzCCf80130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}