@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4> .
@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:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_head {
  this: np:hasAssertion dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_assertion;
    np:hasProvenance dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_provenance;
    np:hasPublicationInfo dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_assertion a np:Assertion .
  
  dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_provenance a np:Provenance .
  
  dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_assertion {
  miriam-gene:268 a ncit:C16612 .
  
  lld:C0010417 a ncit:C7057 .
  
  dgn-gda:DGN8e856f7ba03c3f717671f7a399d607ed sio:SIO_000628 miriam-gene:268, lld:C0010417;
    a sio:SIO_001121 .
}

dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_provenance {
  dgn-np:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_assertion dcterms:description
      "[In this report, the expression of the anti-Mullerian hormone receptor type 2 (AMHR2), the specific receptor of AMH, on the AT was investigated in connection with different urological disorders, such as hernia inguinalis, torsion of AT, cysta epididymis, varicocele, hydrocele testis and various forms of undescended testis.]. 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:23291863;
    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:NP360381.RAVOn1XUFuZ8Fzuz_pOSBUMZRkVtnbmItj3Df27WPU5o4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:31+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" .
}