@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_head {
  this: np:hasAssertion dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_assertion;
    np:hasProvenance dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_provenance;
    np:hasPublicationInfo dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_assertion a np:Assertion .
  
  dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_provenance a np:Provenance .
  
  dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_assertion {
  miriam-gene:864 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN212e74d70073c287c53817ea4d84b3f8 sio:SIO_000628 miriam-gene:864, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_provenance {
  dgn-np:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_assertion dcterms:description
      "[These findings suggest that individuals with this SMAD7 variant that develop CRC are more probably to have tumors with greater invasiveness and methylation of RUNX3, which potentially contributes to their poorer observed survival.]. 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:23104301;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP286145.RAEIk6X809EyfL0HCLSMpVPDY8lkCdbjr-rbFiBvzgOrc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:23+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}