@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE> .
@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:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_head {
  this: np:hasAssertion dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_assertion;
    np:hasProvenance dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_provenance;
    np:hasPublicationInfo dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_assertion a np:Assertion .
  
  dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_provenance a np:Provenance .
  
  dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_assertion {
  miriam-gene:10046 a ncit:C16612 .
  
  lld:C2751824 a ncit:C7057 .
  
  dgn-gda:DGNe9c01841a2229895d7908cfd89f3f981 sio:SIO_000628 miriam-gene:10046, lld:C2751824;
    a sio:SIO_001121 .
}

dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_provenance {
  dgn-np:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_assertion dcterms:description
      "[Mutations in chromosome X open reading frame 6 (CXorf6), a recently described candidate gene involved in the development of male genitalia, have been found in patients with complex 46,XY disorders of sexual development (46,XY DSD) including micropenis, bifid scrotum, and penoscrotal hypospadias.]. 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:18635673;
    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:NP522652.RA43Rs2qaXKX7woIEh7gBpSY1bWrtM-U21nOkDQzFr6hE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}