@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_head {
  this: np:hasAssertion dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion;
    np:hasProvenance dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance;
    np:hasPublicationInfo dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion a np:Assertion .
  
  dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance a np:Provenance .
  
  dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion {
  miriam-gene:6736 a ncit:C16612 .
  
  lld:C0018055 a ncit:C7057 .
  
  dgn-gda:DGNa8b38a988c08d53336103db906480d5a sio:SIO_000628 miriam-gene:6736, lld:C0018055;
    a sio:SIO_001121 .
}

dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_provenance {
  dgn-np:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_assertion dcterms:description
      "[To investigate the presence of mutations in the open reading frame (ORF), as well as on the 5' and 3', flanking regions of the SRY gene in patients with mixed gonadal dysgenesis (MGD) or with Turner syndrome (TS) and Y mosaicism.]. 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:15223166;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP226835.RALJzF6uRhUo7gZsi2nmqj1HADkQr0ijLma2DMW5iSAA8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:06+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}