@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU> .
@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:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_head {
  this: np:hasAssertion dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_assertion;
    np:hasProvenance dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_provenance;
    np:hasPublicationInfo dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_assertion a np:Assertion .
  
  dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_provenance a np:Provenance .
  
  dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN3b16b5586208d86d1c3347d5dacbc130 sio:SIO_000628 miriam-gene:324, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_provenance {
  dgn-np:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_assertion dcterms:description
      "[Germline mutations in the adenomatous polyposis coli (APC) gene cause familial adenomatous polyposis (FAP), an autosomal dominant disease characterized by hundreds to thousands of adenomatous polyps in the colon and rectum, with progression to 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:18406876;
    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:NP155728.RA6OUGtkBOlwT0Rqv1HJLVCYIRZaV9pA4MPStJB3CBNiU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}