@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI> .
@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:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_head {
  this: np:hasAssertion dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_assertion;
    np:hasProvenance dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_provenance;
    np:hasPublicationInfo dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_assertion a np:Assertion .
  
  dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_provenance a np:Provenance .
  
  dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_assertion {
  miriam-gene:4953 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN5111f661d4eae449c161e213d87536bf sio:SIO_000628 miriam-gene:4953, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_provenance {
  dgn-np:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_assertion dcterms:description
      "[Because mutation of ODC in primary human hepatocellular carcinoma has been reported, we examined whether the genetic alterations, such as mutations or structural alterations of the gene, also account for the alteration of ODC activity in human colorectal cancer.]. 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:12148577;
    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:NP504989.RA8ExtOpetPzc3pc9SbYYq_OPKG5Xq7HduQCtaZnuzHqI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:01+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" .
}