@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ> .
@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:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_head {
  this: np:hasAssertion dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_assertion;
    np:hasProvenance dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_provenance;
    np:hasPublicationInfo dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_assertion a np:Assertion .
  
  dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_provenance a np:Provenance .
  
  dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_assertion {
  miriam-gene:3690 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGN894a4907c3de830e558d2ab51d1aa432 sio:SIO_000628 miriam-gene:3690, lld:C0004352;
    a sio:SIO_001121 .
}

dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_provenance {
  dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_assertion dcterms:description
      "[The integrin beta3 (ITGB3) and serotonin transporter (SLC6A4) genes were both recently identified as male quantitative trait loci (QTLs) for serotonin levels and alleles of each have been associated with autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:16721604;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP20545.RAnFIxCFf664j-FAv0FWgxR30tqZ9fPneHrfHZ4_vL9PQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:08+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" .
}