@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU> .
@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:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_head {
  this: np:hasAssertion dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_assertion;
    np:hasProvenance dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_provenance;
    np:hasPublicationInfo dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_assertion a np:Assertion .
  
  dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_provenance a np:Provenance .
  
  dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_assertion {
  miriam-gene:10046 a ncit:C16612 .
  
  lld:C0452147 a ncit:C7057 .
  
  dgn-gda:DGN8c4344809d06e0d4a0ef19bed4b3b8ea sio:SIO_000628 miriam-gene:10046, lld:C0452147;
    a sio:SIO_001121 .
}

dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_provenance {
  dgn-np:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_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:NP630071.RArPXofi9gKSQ4eF9BSaeeDU5UPTJ2cvfy6dZ7jQw7CeU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:20+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" .
}