@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_assertion
a
np:Assertion
.
dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_provenance
a
np:Provenance
.
dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_assertion
{
miriam-gene:84628
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNd03baa6b39712674f888d377adc441c2
sio:SIO_000628
miriam-gene:84628
,
lld:C0036341
;
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sio:SIO_001121
.
}
dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_provenance
{
dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_assertion
dcterms:description
"[These data implicate NTNG1 and NTNG2 in the pathophysiology of schizophrenia and bipolar disorder, but do not support the hypothesis that altered mRNA expression is the mechanism by which genetic variation of NTNG1 or NTNG2 may confer disease susceptibility.]. 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:17507910
;
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:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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