@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA> .
@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/v3.0.0/void/> .

dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_head {
  this: np:hasAssertion dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_assertion;
    np:hasProvenance dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_provenance;
    np:hasPublicationInfo dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_assertion a np:Assertion .
  
  dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_provenance a np:Provenance .
  
  dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0206646 a ncit:C7057 .
  
  dgn-gda:DGNa58a077fa6dd33c32fdcbc107e6fc03f sio:SIO_000628 miriam-gene:324, lld:C0206646;
    a sio:SIO_001122 .
}

dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_provenance {
  dgn-np:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_assertion dcterms:description
      "[Our analysis confirms 3 APC mutation to be the most significant risk factor for IAD development. The independent association between positive FH and IAD risk suggests the existence of modifier genes, independent of the APC genotype-phenotype correlation. ]. 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:20352275;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP135765.RAMsMzIrs57NV7KRCPt0hraBq8KTzFt347M4lx00ypIFA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:56+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}