@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ> .
@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:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_head {
  this: np:hasAssertion dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_assertion;
    np:hasProvenance dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_provenance;
    np:hasPublicationInfo dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_assertion a np:Assertion .
  
  dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_provenance a np:Provenance .
  
  dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_assertion {
  miriam-gene:5530 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGNa073612622d5e1629d80136c59d1a188 sio:SIO_000628 miriam-gene:5530, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_provenance {
  dgn-np:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_assertion dcterms:description
      "[Although chromosomal structural anomaly is presumed to play an important role in the carcinogenesis of CRC, chromosomal copy number alterations (CNA) and loss of heterozygosity (LOH) have not yet been analyzed extensively at high resolution in CRC.]. 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:18564138;
    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:NP706703.RAis1fTSIMH3P1vW18_JBE7K60eI4Gjz1eNL0Fyep4uUQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:09+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" .
}