@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE> .
@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:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_head {
  this: np:hasAssertion dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_assertion;
    np:hasProvenance dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_provenance;
    np:hasPublicationInfo dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_assertion a np:Assertion .
  
  dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_provenance a np:Provenance .
  
  dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_assertion {
  miriam-gene:79947 a ncit:C16612 .
  
  lld:C1263846 a ncit:C7057 .
  
  dgn-gda:DGN9475a0ddfd9c0321890c5e7866d51186 sio:SIO_000628 miriam-gene:79947, lld:C1263846;
    a sio:SIO_001121 .
}

dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_provenance {
  dgn-np:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_assertion dcterms:description
      "[The use of the Continuous Performance Test (CPT), as an endophenotypic measure, is valuable for genetic studies because it may show increased sensitivity to specific dimensions in attention deficit hyperactivity disorder.]. 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:14584093;
    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:NP538809.RAd2gCBcbG9XRQO90OaJ2MXXTC6Lqr1ABdtQlGCbYBYHE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:25+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" .
}