@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs> .
@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:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_head {
  this: np:hasAssertion dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_assertion;
    np:hasProvenance dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_provenance;
    np:hasPublicationInfo dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_assertion a np:Assertion .
  
  dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_provenance a np:Provenance .
  
  dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_assertion {
  miriam-gene:3481 a ncit:C16612 .
  
  lld:C0175754 a ncit:C7057 .
  
  dgn-gda:DGN7c3368d603e6060907fdc2d196bf4773 sio:SIO_000628 miriam-gene:3481, lld:C0175754;
    a sio:SIO_001121 .
}

dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_provenance {
  dgn-np:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_assertion dcterms:description
      "[Although ACC is extremely rare, recent advances in genomic and expression profiling, coupled with knowledge gained from the study of the inherited syndromes that increase ACC risk, are beginning to bring together a picture of a tumor type dependent on p53, the G2/M cell cycle transition and IGF2 stimulation.]. 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:19519204;
    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:NP744735.RAq8SiLz63bRT2S6unY8dAopjJ6fDF1w4bguDEWuyqgxs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:22+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" .
}