@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#> .

dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_head {
  this: np:hasAssertion dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_assertion;
    np:hasProvenance dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_provenance;
    np:hasPublicationInfo dgn-np:NP574074.RAcs4kVTDqsCCI2ux4R3bvq-EzyBhcsaTrH71A0Uik4rY130_publicationInfo;
    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;
    a 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 .
}

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 <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}