@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk> .
@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:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_head {
  this: np:hasAssertion dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_assertion;
    np:hasProvenance dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_provenance;
    np:hasPublicationInfo dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_assertion a np:Assertion .
  
  dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_provenance a np:Provenance .
  
  dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  
  lld:C0567439 a ncit:C7057 .
  
  dgn-gda:DGNacd28643dcd2c7cb0d802f2ef31e8ea9 sio:SIO_000628 miriam-gene:4221, lld:C0567439;
    a sio:SIO_001121 .
}

dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_provenance {
  dgn-np:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_assertion dcterms:description
      "[Similarly, there is little evidence to suggest that the mutations involved in genetic syndromes associated with pituitary tumors (such as the gsp, MEN1, PKAR1A or AIP mutations) are common in sporadic tumors.]. 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:19058014;
    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:NP468769.RAqUv4rf8s2_PTz06BwQWNmTS0T4LLLN_Tq6ceUoX_THk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:41+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" .
}