@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg> .
@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:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_head {
  this: np:hasAssertion dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion;
    np:hasProvenance dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance;
    np:hasPublicationInfo dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion a np:Assertion .
  
  dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance a np:Provenance .
  
  dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion {
  miriam-gene:57697 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN66da302c5b8c9f81c2a5b251401f9ac0 sio:SIO_000628 miriam-gene:57697, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance {
  dgn-np:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion dcterms:description
      "[We sought somatic mutations in the corresponding genes in the CRCs of the patients harboring the germline lesions and found biallelic inactivation of FANCM, LAMB4, PTCHD3, LAMC3, and TREX2, potentially implicating these genes as tumor suppressors.]. 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:23585368;
    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:NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:09+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" .
}