@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU> .
@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:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_head {
  this: np:hasAssertion dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_assertion ;
    np:hasProvenance dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_provenance ;
    np:hasPublicationInfo dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_assertion a np:Assertion .
  dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_provenance a np:Provenance .
  dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_assertion {
  miriam-gene:367 a ncit:C16612 .
  lld:C0021364 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_provenance {
  dgn-np:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_assertion dcterms:description "[Although CAIS is the best known phenotype, recent studies from our laboratory and elsewhere show that malfunction of the AR is associated with many androgen-regulated diseases or conditions that cross traditional clinical disciplines ranging from paediatrics (ambiguous genitalia), gynaecology (primary amenorrhoea), urology (prostate cancer), neurology (spinal bulbar muscular atrophy), reproductive medicine (male infertility), orthopedics (rheumatoid arthritis), oncology (breast cancer) and dermatology (hirsutism, baldness and acne).]. 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:10711573 ;
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  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:NP277639.RAiO_pmFey2_AtTtiMNyzfJByP2-MkCDouFkLkPC915GU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:51+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}