@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_head
{
this:
np:hasAssertion
dgn-np:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_assertion
a
np:Assertion
.
dgn-np:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_provenance
a
np:Provenance
.
dgn-np:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:91752
a
ncit:C16612
.
lld:C0033975
a
ncit:C7057
.
dgn-gda:DGN4c97c398c3ff406ddd939177b518e9cb
sio:SIO_000628
miriam-gene:91752
,
lld:C0033975
;
a
sio:SIO_001121
.
}
dgn-np:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_provenance
{
dgn-np:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_assertion
dcterms:description
"[To (1) assess the association between SNPs in ZNF804A and the ZNF804A polygenic score with measures of cognition in cases with psychosis and (2) assess whether epistasis within the ZNF804A pathway could explain additional variation above and beyond that explained by the polygenic score.]. 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:24828433
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP960917.RAHv-zLALilZlfMInNRQybWRoGQmU31u7pcC5USFMYWaI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:27+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
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;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}