@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8> .
@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:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_head {
  this: np:hasAssertion dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_assertion;
    np:hasProvenance dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_provenance;
    np:hasPublicationInfo dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_assertion a np:Assertion .
  
  dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_provenance a np:Provenance .
  
  dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGN65be30a41a547b82c31c53471147d56d sio:SIO_000628 miriam-gene:1636, lld:C0032580;
    a sio:SIO_001122 .
}

dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_provenance {
  dgn-np:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_assertion dcterms:description
      "[ The severity of colonic FAP may be modified by alleles at the NAT1 and/or NAT2 loci. The identity of any functional variation remains unknown as NAT1*10 appears to be non-functional and there is linkage disequilibrium between alleles at multiple sites within these loci which are adjacent on chromosome 8p22. While evidence from this study cannot be conclusive, our data suggest that NAT1 and NAT2 variants may explain an approximately twofold increase in polyp number in the FAP colon.]. 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:14724163;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP49564.RAvwvcPo7ZZJNY7wrMhdd_BuXGJ61e8JF1eXjKnmxpPS8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}