@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8> .
@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:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_head {
  this: np:hasAssertion dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_assertion;
    np:hasProvenance dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_provenance;
    np:hasPublicationInfo dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_assertion a np:Assertion .
  
  dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_provenance a np:Provenance .
  
  dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_assertion {
  miriam-gene:9869 a ncit:C16612 .
  
  lld:C0007102 a ncit:C7057 .
  
  dgn-gda:DGN0adb9bd7770fffbb9e123a308bfe7b2f sio:SIO_000628 miriam-gene:9869, lld:C0007102;
    a sio:SIO_001121 .
}

dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_provenance {
  dgn-np:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_assertion dcterms:description
      "[Activation of Notch1 converted high-grade adenoma into low-grade adenoma in an Apcmin mouse colon cancer model and suppressed the expression of WNT target genes in human colorectal cancer cells through epigenetic modification recruiting histone methyltransferase SET domain bifurcated 1 (SETDB1).]. 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:22863622;
    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:NP787172.RAl_VTPeIrcS8ScvV6nZC9XrtWVhdaexWEKUba23zrIi8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}