@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA> .
@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:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_head {
  this: np:hasAssertion dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_assertion;
    np:hasProvenance dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_provenance;
    np:hasPublicationInfo dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_assertion a np:Assertion .
  
  dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_provenance a np:Provenance .
  
  dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0936016 a ncit:C7057 .
  
  dgn-gda:DGN03106d943a32afb10b34e7c94c459186 sio:SIO_000628 miriam-gene:367, lld:C0936016;
    a sio:SIO_001121 .
}

dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_provenance {
  dgn-np:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_assertion dcterms:description
      "[Alterations in the androgen sensitivity pathway have been identified in severely undermasculinized boys, and mutations of the androgen receptor gene (AR) are usually found in partial or complete androgen insensitivity syndrome (AIS).]. 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:23637914;
    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:NP250916.RAOz-0wa9ptKiEccnpbgXsi-1abEfHcb83WrNHNGW7wFA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:02+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" .
}