@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0> .
@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:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_head {
  this: np:hasAssertion dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_assertion;
    np:hasProvenance dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_provenance;
    np:hasPublicationInfo dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_assertion a np:Assertion .
  
  dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_provenance a np:Provenance .
  
  dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_assertion {
  miriam-gene:231 a ncit:C16612 .
  
  lld:C0848558 a ncit:C7057 .
  
  dgn-gda:DGN68e2ae615c6a70974e7f8b3bcb7ae912 sio:SIO_000628 miriam-gene:231, lld:C0848558;
    a sio:SIO_001122 .
}

dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_provenance {
  dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_assertion dcterms:description
      "[ This finding is in accordance with the assumption that functional polymorphisms may play an important role in complex disorders such as hypospadias when several genes as well as environmental factors contribute to the etiology.]. 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:16174723;
    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:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}