@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE> .
@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:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_head {
  this: np:hasAssertion dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_assertion;
    np:hasProvenance dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_provenance;
    np:hasPublicationInfo dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_assertion a np:Assertion .
  
  dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_provenance a np:Provenance .
  
  dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0001430 a ncit:C7057 .
  
  dgn-gda:DGN83c261957d8368d457d66b459e088384 sio:SIO_000628 miriam-gene:324, lld:C0001430;
    a sio:SIO_001121 .
}

dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_provenance {
  dgn-np:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_assertion dcterms:description
      "[Based on the association of APC missense variants with multiple adenomas, we proposed that much of this may be due to the cumulative effects of low frequency, low penetrance variants, and the rare variant hypothesis.]. 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:16596323;
    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:NP543693.RAz5bqmmfxleYb1ZS73W-ebfbwkoRdQwh2Ypg-BGIdjqE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:51+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: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" .
}