@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw> .
@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:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_head {
  this: np:hasAssertion dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_assertion;
    np:hasProvenance dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_provenance;
    np:hasPublicationInfo dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_assertion a np:Assertion .
  
  dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_provenance a np:Provenance .
  
  dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_assertion {
  miriam-gene:10249 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGN2eac0d0d1066108242f9317bc2b587e1 sio:SIO_000628 miriam-gene:10249, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_provenance {
  dgn-np:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_assertion dcterms:description
      "[Human mapping studies have shown that the aniridia (AN2) gene, which is part of the Wilms tumor susceptibility, aniridia, genitourinary abnormalities, and mental retardation (WAGR) complex, is also between FSHB and CAT on human chromosome 11.]. 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:2347591;
    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:NP1059303.RAoNEw3touhL9ExnJoaWNOOkKL0xFZJGfp78LR6oS12yw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:46+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" .
}