@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro> .
@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:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_head {
  this: np:hasAssertion dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_assertion;
    np:hasProvenance dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_provenance;
    np:hasPublicationInfo dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_assertion a np:Assertion .
  
  dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_provenance a np:Provenance .
  
  dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_assertion {
  miriam-gene:4095 a ncit:C16612 .
  
  lld:C0525045 a ncit:C7057 .
  
  dgn-gda:DGNa69a5b67e769c3e0d6798158fc94541c sio:SIO_000628 miriam-gene:4095, lld:C0525045;
    a sio:SIO_001121 .
}

dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_provenance {
  dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_assertion dcterms:description
      "[The findings of anticipation in this study of families with UPAD and previous findings in families with BPAD suggest that the variable expression of unstable expansions of trinucleotide repeats may turn out to be the basis of the continuum of liability in affective 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:8557885;
    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:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:06+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" .
}