@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I> .
@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:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_head {
  this: np:hasAssertion dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_assertion;
    np:hasProvenance dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_provenance;
    np:hasPublicationInfo dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_assertion a np:Assertion .
  
  dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_provenance a np:Provenance .
  
  dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0153381 a ncit:C7057 .
  
  dgn-gda:DGNc54e0e98a2fa0c32d025303d8b91fa78 sio:SIO_000628 miriam-gene:324, lld:C0153381;
    a sio:SIO_001121 .
}

dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_provenance {
  dgn-np:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_assertion dcterms:description
      "[Because of similar causes of oral and esophageal cancers, we investigated allelic deletion of the adenomatous polyposis coli gene in oral cancers by examining tumor cells of persons normally heterozygous at a polymorphic restriction site in adenomatous polyposis coli.]. 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:8170656;
    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:NP488026.RAerXfTaLUsHxJS8XwTWMKr8Tgxgz2P6irP5WSftSev3I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:51+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" .
}