@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ> .
@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:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_head {
  this: np:hasAssertion dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_assertion;
    np:hasProvenance dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_provenance;
    np:hasPublicationInfo dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_assertion a np:Assertion .
  
  dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_provenance a np:Provenance .
  
  dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGNbe921f3ebd4d903a8b3a77fe213f67be sio:SIO_000628 miriam-gene:3342, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_provenance {
  dgn-np:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_assertion dcterms:description
      "[As a first step toward understanding the underlying genetic changes and determining early chromosomal changes of tumor development in this population, we used comparative genomic hybridization (CGH) to screen for losses and gains of DNA sequences along chromosomes in 20 morphologically normal tumor surroundings (MNTS) and 40 CRC tissues from 40 patients.]. 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:15993271;
    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:NP587449.RAb8aQ5RCnoUomneCesAehwlOKVUhe_v_IfJrmWbdS2lQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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" .
}