@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU> .
@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:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_head {
  this: np:hasAssertion dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_assertion;
    np:hasProvenance dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_provenance;
    np:hasPublicationInfo dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_assertion a np:Assertion .
  
  dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_provenance a np:Provenance .
  
  dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_assertion {
  miriam-gene:7166 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGNb642abc6392325ff4752434b946dfc02 sio:SIO_000628 miriam-gene:7166, lld:C0004352;
    a sio:SIO_001122 .
}

dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_provenance {
  dgn-np:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_assertion dcterms:description
      "[The role in autism etiology of seven candidate genes in the serotonin metabolic and neurotransmission pathways and mapping to autism linkage regions (SLC6A4, HTR1A, HTR1D, HTR2A, HTR5A, TPH1 and ITGB3) was analyzed in a sample of 186 nuclear families.]. 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:17203304;
    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:NP66829.RAdDr5U9ONbcDMUHS9b3_HQynmhbYQzH4DAQ4hp0NrUlU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}