@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8> .
@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:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_head {
  this: np:hasAssertion dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_assertion;
    np:hasProvenance dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_provenance;
    np:hasPublicationInfo dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_assertion a np:Assertion .
  
  dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_provenance a np:Provenance .
  
  dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_assertion {
  miriam-gene:1027 a ncit:C16612 .
  
  lld:C0032019 a ncit:C7057 .
  
  dgn-gda:DGN319fb49dfb47d04d57c54cdd104efd26 sio:SIO_000628 miriam-gene:1027, lld:C0032019;
    a sio:SIO_001121 .
}

dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_provenance {
  dgn-np:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_assertion dcterms:description
      "[The genetic causes of common pituitary tumors remain for the most part unknown; progress has been limited to the elucidation of the molecular etiology of four genetic syndromes predisposing to pituitary neoplasias: McCune-Albright syndrome, multiple endocrine neoplasia type 1, Carney complex and, most recently, familial acromegaly and prolactinomas and other tumors caused by mutations in the GNAS, menin, PRKAR1A, AIP, and p27 (CDKN1B) genes, respectively.]. 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:17613552;
    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:NP451958.RAd994QIoPhSwjWol4YPCUl6v_qWc2rcXAAwotah-BfH8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}