@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c> .
@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:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_head {
  this: np:hasAssertion dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_assertion;
    np:hasProvenance dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_provenance;
    np:hasPublicationInfo dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_assertion a np:Assertion .
  
  dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_provenance a np:Provenance .
  
  dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_assertion {
  miriam-gene:6445 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN0d82d0ab11a748c44f74f59288239c73 sio:SIO_000628 miriam-gene:6445, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_provenance {
  dgn-np:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_assertion dcterms:description
      "[We find that somatic mutations create or disrupt putative miRNA target sites in the 3'UTRs of many genes, including several genes, such as MITF, EPHA3, TAL1, SCG3, and GSDMA, which have been previously associated with 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:23091610;
    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:NP745339.RAChDRYdFUaxrTPMmh_oSz6eJ-2ieRdjWLRDpC1ig8z_c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:32+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" .
}