@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk> .
@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/v4.0.0/void/> .

dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_head {
  this: np:hasAssertion dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_assertion;
    np:hasProvenance dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_provenance;
    np:hasPublicationInfo dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_assertion a np:Assertion .
  
  dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_provenance a np:Provenance .
  
  dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0936016 a ncit:C7057 .
  
  dgn-gda:DGN35fe864b12eca46d8e009ab52264f0d8 sio:SIO_000628 miriam-gene:367, lld:C0936016;
    a sio:SIO_001121 .
}

dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_provenance {
  dgn-np:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_assertion dcterms:description
      "[This review discusses the various AR gene mutations found in androgen insensitivity syndrome (AIS) and the other conditions described above, and relates how different mutations, or disruption of different functional domains, contributes to the various phenotypes.]. 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:7489816;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1308654.RAIs1sJTgbe7EoeZSthLu7xt4HFp5v53a1NXWsu9AfFOk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:39+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}