@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U> .
@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:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_head {
  this: np:hasAssertion dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_assertion;
    np:hasProvenance dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_provenance;
    np:hasPublicationInfo dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_assertion a np:Assertion .
  
  dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_provenance a np:Provenance .
  
  dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  
  lld:C2939420 a ncit:C7057 .
  
  dgn-gda:DGN5456cbaea51b530719764f3eeda17180 sio:SIO_000628 miriam-gene:4221, lld:C2939420;
    a sio:SIO_001121 .
}

dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_provenance {
  dgn-np:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_assertion dcterms:description
      "[Previous molecular studies have shown that gain of chromosome 9q rather than MEN1 gene mutation is an important early event in tumour development and that chromosomal instability is associated with metastatic disease.]. 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:17068744;
    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:NP168390.RA0O8Y1fYBr_A90MiP-ycgVwMr7wFCOp8VMng6D6l-e3U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}