@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM> .
@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:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_head {
  this: np:hasAssertion dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_assertion;
    np:hasProvenance dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_provenance;
    np:hasPublicationInfo dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_assertion a np:Assertion .
  
  dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_provenance a np:Provenance .
  
  dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0039585 a ncit:C7057 .
  
  dgn-gda:DGN5c2bd8b4984ba2300a187d9a98d54922 sio:SIO_000628 miriam-gene:367, lld:C0039585;
    a sio:SIO_001121 .
}

dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_provenance {
  dgn-np:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_assertion dcterms:description
      "[To screen for point mutations in the AR gene underlying the phenotypic abnormalities in the androgen insensitivity syndrome (AIS), the eight exons of the AR gene were amplified from genomic DNA using the polymerase chain reaction (PCR) and analyzed by denaturing gradient gel electrophoresis.]. 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:1480178;
    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:NP431030.RAasPMCJjCAs0hHuNAFVl6sKAR9NAPOcSKnTBr0PiVHsM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:00+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" .
}