@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q> .
@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:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_head {
  this: np:hasAssertion dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_assertion;
    np:hasProvenance dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_provenance;
    np:hasPublicationInfo dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_assertion a np:Assertion .
  
  dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_provenance a np:Provenance .
  
  dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_assertion {
  miriam-gene:2618 a ncit:C16612 .
  
  lld:C0039585 a ncit:C7057 .
  
  dgn-gda:DGN0cbfb6b13eae832e9e08e89522817328 sio:SIO_000628 miriam-gene:2618, lld:C0039585;
    a sio:SIO_001121 .
}

dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_provenance {
  dgn-np:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_assertion dcterms:description
      "[Establishing the functional consequences of androgen receptor mutations in vitro systems and correlating them with clinical presentation may ultimately provide an explanation for the variable clinical presentation of AIS and perhaps enable prediction of the response to androgen therapy in infants with PAIS.]. 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:8733002;
    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:NP686965.RAVdN0cGerKTU_-2sRh8b521dcmXPYv6Zj0izNuA7Mf7Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:57+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" .
}