@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo> .
@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:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_head {
  this: np:hasAssertion dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_assertion;
    np:hasProvenance dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_provenance;
    np:hasPublicationInfo dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_assertion a np:Assertion .
  
  dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_provenance a np:Provenance .
  
  dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0035335 a ncit:C7057 .
  
  dgn-gda:DGN7868ee88f246bf4c619955d837aca449 sio:SIO_000628 miriam-gene:1956, lld:C0035335;
    a sio:SIO_001121 .
}

dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_provenance {
  dgn-np:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_assertion dcterms:description
      "[Multiple genetic changes, including the gene amplification of bcl-1, epidermal growth factor receptor, and c-myc, and the loss of heterozygosity of multiple tumor suppressor genes, including retinoblastoma, mutated in colorectal carcinoma, adenomatous polyposis coli, and deleted in colorectal carcinoma, in each case were investigated and the frequency of genetic alterations compared between both groups.]. 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:10357400;
    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:NP350792.RArDStti-5yRAo59g8rBleN4uhq1HEWhphi1PXDNBsISo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:26+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" .
}