@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU> .
@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:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_head {
  this: np:hasAssertion dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_assertion;
    np:hasProvenance dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_provenance;
    np:hasPublicationInfo dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_assertion a np:Assertion .
  
  dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_provenance a np:Provenance .
  
  dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_assertion {
  miriam-gene:6532 a ncit:C16612 .
  
  lld:C0236792 a ncit:C7057 .
  
  dgn-gda:DGN6ad661d1118320948f129f971cf81eed sio:SIO_000628 miriam-gene:6532, lld:C0236792;
    a sio:SIO_001121 .
}

dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_provenance {
  dgn-np:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_assertion dcterms:description
      "[As two individuals with SERT I425V and OCD also had Asperger syndrome (AS), an autism spectrum disorder, and as other rare SERT variants have recently shown significant associations with autism, we set out to extend our original OCD study by genotyping additional autism/AS and OCD samples.]. 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:18197083;
    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:NP30088.RA2DPG_b8286KsZrozlmvSP9KguboZLKrfTA2Qza51KIU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:13+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" .
}