@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_head {
  this: np:hasAssertion dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_assertion;
    np:hasProvenance dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_provenance;
    np:hasPublicationInfo dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_assertion a np:Assertion .
  
  dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_provenance a np:Provenance .
  
  dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_assertion {
  miriam-gene:5021 a ncit:C16612 .
  
  lld:C0033038 a ncit:C7057 .
  
  dgn-gda:DGN99f629d677d3d7a31aa8de97c742b114 sio:SIO_000628 miriam-gene:5021, lld:C0033038;
    a sio:SIO_001122 .
}

dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_provenance {
  dgn-np:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_assertion dcterms:description
      "[• We found a heterozygote effect on one SNP in the oxytocin receptor gene (rs75775), so that individuals heterozygous for this SNP had significantly elevated risk for premature ejaculation symptoms compared with carriers of either homozygote.]. 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:22882465;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1004261.RASj-VPbbudUrHRVMSmWnfU9t2eFIO3jXpokJaHHTW2tI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:21+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}