@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY> .
@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:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_head {
  this: np:hasAssertion dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_assertion;
    np:hasProvenance dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_provenance;
    np:hasPublicationInfo dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_assertion a np:Assertion .
  
  dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_provenance a np:Provenance .
  
  dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_assertion {
  miriam-gene:6535 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGNbc1a38e12152ab14ca21a92114569666 sio:SIO_000628 miriam-gene:6535, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_provenance {
  dgn-np:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_assertion dcterms:description
      "[The purpose of our study was to screen 100 male subjects with autism spectrum disorder for mutations in the SLC6A8 gene in order to determine the frequency of this genetic disorder in this population.]. 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:18461508;
    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:NP526134.RArf4swRfkYz3n-nTQ3bsMJbx0gy-jIufU4X_run3VQcY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:15+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" .
}