@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U> .
@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:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_head {
  this: np:hasAssertion dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_assertion;
    np:hasProvenance dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_provenance;
    np:hasPublicationInfo dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_assertion a np:Assertion .
  
  dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_provenance a np:Provenance .
  
  dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_assertion {
  miriam-gene:4853 a ncit:C16612 .
  
  lld:C0009404 a ncit:C7057 .
  
  dgn-gda:DGNbddb3f4a81e8255b12503b4b14a1cd10 sio:SIO_000628 miriam-gene:4853, lld:C0009404;
    a sio:SIO_001121 .
}

dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_provenance {
  dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_assertion dcterms:description
      "[We find large and small chromothripsis events in nearly every colorectal tumor sample and show that several breakpoints of chromothripsis clusters and isolated rearrangements affect cancer genes, including NOTCH2, EXO1 and MLL3.]. 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:22014273;
    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:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}