@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA
> .
@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:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_head
{
this:
np:hasAssertion
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_assertion
;
np:hasProvenance
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_provenance
;
np:hasPublicationInfo
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_assertion
a
np:Assertion
.
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_provenance
a
np:Provenance
.
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_assertion
{
miriam-gene:5173
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN4bddd1a5024229203a15859d48769ba3
sio:SIO_000628
miriam-gene:5173
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_provenance
{
dgn-np:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_assertion
dcterms:description
"[We conclude that PDYN gene polymorphism alone does not alter the risk for schizophrenia but, by an epistatic interaction with the Gly allele of DRD3 gene, may contribute to the susceptibility to this disorder.]. 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:12207142
;
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:NP53249.RAHFg2QizZ_0NbIdg_Wtjl60sxfyDTI0kz13GBFMVanvA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}