@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw> .
@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/v4.0.0/void/> .

dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_head {
  this: np:hasAssertion dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_assertion;
    np:hasProvenance dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_provenance;
    np:hasPublicationInfo dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_assertion a np:Assertion .
  
  dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_provenance a np:Provenance .
  
  dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_assertion {
  miriam-gene:4645 a ncit:C16612 .
  
  lld:C1263846 a ncit:C7057 .
  
  dgn-gda:DGN3e35953646aff719500d849c09a971c3 sio:SIO_000628 miriam-gene:4645, lld:C1263846;
    a sio:SIO_001121 .
}

dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_provenance {
  dgn-np:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_assertion dcterms:description
      "[We therefore wanted to examine whether the reported BD genetic variants in CACNA1C, ANK3, MYO5B, TSPAN8 and ZNF804A loci are associated with ADHD or with scores on the Mood Disorder Questionnaire (MDQ), a commonly used screening instrument for bipolar spectrum disorders.]. 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:21276201;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP868559.RAMHa4zJwQc3c_ahNm6Y27DZg_O4oQLWqcB1vmGDMDkCw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:18+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}