@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY> .
@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/v3.0.0/void/> .

dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_head {
  this: np:hasAssertion dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_assertion;
    np:hasProvenance dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_provenance;
    np:hasPublicationInfo dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_assertion a np:Assertion .
  
  dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_provenance a np:Provenance .
  
  dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_assertion {
  miriam-gene:6736 a ncit:C16612 .
  
  lld:C0206661 a ncit:C7057 .
  
  dgn-gda:DGN14a144ce8039e9b65043432890e45115 sio:SIO_000628 miriam-gene:6736, lld:C0206661;
    a sio:SIO_001121 .
}

dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_provenance {
  dgn-np:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_assertion dcterms:description
      "[Our results suggest that lack of a second sex chromosome in majority cells of the patient may have triggered the short stature and primary infertility, and the mutated SRY protein may be associated with the development of gonadoblastoma.]. 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:20849656;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP713089.RA33cOukOmuHaGfds2WO8dd5w_eGpXe1JrbWur46FEXYY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:50+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}