@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg> .
@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:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_head {
  this: np:hasAssertion dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_assertion;
    np:hasProvenance dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_provenance;
    np:hasPublicationInfo dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_assertion a np:Assertion .
  
  dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_provenance a np:Provenance .
  
  dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_assertion {
  miriam-gene:9968 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN9bd825da5fa6ccef4679ecfdccb8d881 sio:SIO_000628 miriam-gene:9968, lld:C0036341;
    a sio:SIO_001122 .
}

dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_provenance {
  dgn-np:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_assertion dcterms:description
      "[Taken together, these findings further refine the behavioral endophenotype associated with the HOPA(12bp) allele and suggest that the sequence surrounding HOPA may need to be considered to fully understand the molecular basis of the phenotype associated with the HOPA(12bp) allele.]. 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:15108174;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP54786.RAkxoelYlTuU7ZGav4EIbVYYV6hdGUNudJa92g5Ya6_Lg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}