@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg> .
@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:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_head {
  this: np:hasAssertion dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_assertion;
    np:hasProvenance dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_provenance;
    np:hasPublicationInfo dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_assertion a np:Assertion .
  
  dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_provenance a np:Provenance .
  
  dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_assertion {
  miriam-gene:2516 a ncit:C16612 .
  
  lld:C0018051 a ncit:C7057 .
  
  dgn-gda:DGNa23689be893baf8726a5300b5f7b394f sio:SIO_000628 miriam-gene:2516, lld:C0018051;
    a sio:SIO_001121 .
}

dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_provenance {
  dgn-np:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_assertion dcterms:description
      "[Gonadal dysgenesis may be isolated, as in the case of SRY mutations, or associated with abnormal development of other organs, such as bone or adrenals, consistent with the spatial expression profile of the disrupted genes (SOX9 or SF1).]. 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:11990797;
    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:NP234310.RAXEo3tXenFyxB5uu10Vf6jvUS49137tONxYh5tkePhxg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:11+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" .
}