@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI> .
@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:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_head {
  this: np:hasAssertion dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_assertion;
    np:hasProvenance dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_provenance;
    np:hasPublicationInfo dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_assertion a np:Assertion .
  
  dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_provenance a np:Provenance .
  
  dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_assertion {
  miriam-gene:57152 a ncit:C16612 .
  
  lld:C1263846 a ncit:C7057 .
  
  dgn-gda:DGN72898f93ce10dbbb30f9514132d87a5d sio:SIO_000628 miriam-gene:57152, lld:C1263846;
    a sio:SIO_001121 .
}

dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_provenance {
  dgn-np:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_assertion dcterms:description
      "[In the ADHD patients, ANCOVA revealed that there were no significant differences in the subscales and total score between the ADHD probands with the CC genotype and those with the CG and GG genotypes in ARS and the Continuous Performance Test (CPT) when adjusting for age and gender.]. 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:20470849;
    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:NP168440.RA4UZW2XlgJZRrkqhaeEiMJGZQomRfKVgHDu1NDtqeEAI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}