@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38> .
@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/v4.0.0/void/> .

dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_head {
  this: np:hasAssertion dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_assertion;
    np:hasProvenance dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_provenance;
    np:hasPublicationInfo dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_assertion a np:Assertion .
  
  dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_provenance a np:Provenance .
  
  dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGN303a6cfc5bf4ff78ec415bde73ca424f sio:SIO_000628 miriam-gene:324, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_provenance {
  dgn-np:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_assertion dcterms:description
      "[Mutations of the APC gene are thought to be responsible for the development of FAP, and the location of the mutation on the gene is thought to influence the nature of the extracolonic manifestations that a given patient might develop.]. 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:15592657;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP472424.RAx30D5JkhAd7NpROrl0QBnDC3tdAMJ3vjAfILJKrHp38130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:19+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}