@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A> .
@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:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_head {
  this: np:hasAssertion dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_assertion;
    np:hasProvenance dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_provenance;
    np:hasPublicationInfo dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_assertion a np:Assertion .
  
  dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_provenance a np:Provenance .
  
  dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C0004936 a ncit:C7057 .
  
  dgn-gda:DGNae0a5c6ab37cc9bfc55b9593f8ed5236 sio:SIO_000628 miriam-gene:1312, lld:C0004936;
    a sio:SIO_001121 .
}

dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_provenance {
  dgn-np:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_assertion dcterms:description
      "[Since sex differences in the genetic architecture of brain function and psychiatric disorders are the rule not the exception, we anticipate that additional evidence will emerge for sexual dimorphisms, not only in COMT but also in many other autosomal genes.]. 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:21769726;
    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:NP385842.RAftouevYzrjI9yajV2kvTAcrv_FKZtxrp7FrNQb-s12A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:50+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" .
}