@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4> .
@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:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_head {
  this: np:hasAssertion dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_assertion;
    np:hasProvenance dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_provenance;
    np:hasPublicationInfo dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_assertion a np:Assertion .
  
  dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_provenance a np:Provenance .
  
  dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_assertion {
  miriam-gene:54205 a ncit:C16612 .
  
  lld:C0032927 a ncit:C7057 .
  
  dgn-gda:DGNc75bfcefdc4947c2d31e29d8300f399b sio:SIO_000628 miriam-gene:54205, lld:C0032927;
    a sio:SIO_001121 .
}

dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_provenance {
  dgn-np:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_assertion dcterms:description
      "[HCS, which accounts for approximately 5%-10% of all malignancies, is characterized by diagnosis of the same malignancy in multiple family members, an earlier age of onset than expected, an increased frequency of bilateral cancers in paired organs, and the presence of premalignant syndromes.]. 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:7675683;
    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:NP313761.RAmx34_6ehYQoPnCVf9QMsV4QIDvCJfqfSbG0EVFjX6_4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:00+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" .
}