@prefix dc: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs> .
@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:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_head {
   this: np:hasAssertion dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_assertion ;
    np:hasProvenance dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_provenance ;
    np:hasPublicationInfo dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_assertion a np:Assertion .
  dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_provenance a np:Provenance .
  dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_assertion {
   miriam-gene:22854 a ncit:C16612 .
  lld:C0005586 a ncit:C7057 .
  dgn-gda:DGN0f7b5edcfa4b98ace572a0996fe82d95 sio:SIO_000628 miriam-gene:22854 , lld:C0005586 ;
    a sio:SIO_001121 .
}
dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_provenance {
   dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_assertion dc: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_curated ;
    sio:SIO_000772 miriam-pubmed:17507910 ;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708 ;
    prov:wasGeneratedBy eco:ECO_0000218 .
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  dgn-void:source_evidence_curated a eco:ECO_0000205 ;
    rdfs:comment "Gene-disease associations manually curated."@en ;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}
dgn-np:NP24920.RACYW8nmPGIyJ0kEV3VHhBpOuyz47TeKD0QtS4d69YHQs130_publicationInfo {
   this: dc:created "2014-10-02T12:32:10+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc: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" .
}