@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs> .
@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:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_head {
  this: np:hasAssertion dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_assertion;
    np:hasProvenance dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_provenance;
    np:hasPublicationInfo dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_assertion a np:Assertion .
  
  dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_provenance a np:Provenance .
  
  dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0936016 a ncit:C7057 .
  
  dgn-gda:DGN61a9591bee3abc4257b560d21112bb54 sio:SIO_000628 miriam-gene:367, lld:C0936016;
    a sio:SIO_001121 .
}

dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_provenance {
  dgn-np:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_assertion dcterms:description
      "[When the mutation of the androgen receptor gene has not been identified, Hind III polymorphism of the trophoblastic DNA is useful in the prenatal diagnosis of androgen insensitivity syndrome in high-risk families.]. 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:7910529;
    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:NP1326203.RA_lVJNPb7x-bxTIUIICBlgNy8mqOKKxnKvthsjACVchs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:47+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" .
}