@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg> .
@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:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_head {
  this: np:hasAssertion dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_assertion;
    np:hasProvenance dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_provenance;
    np:hasPublicationInfo dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_assertion a np:Assertion .
  
  dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_provenance a np:Provenance .
  
  dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0086692 a ncit:C7057 .
  
  dgn-gda:DGNefdb614cf038a81167f4d3eec8676766 sio:SIO_000628 miriam-gene:324, lld:C0086692;
    a sio:SIO_001121 .
}

dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_provenance {
  dgn-np:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_assertion dcterms:description
      "[The present results and our previous data on LOH in a recurring desmoid tumor suggest that the heterozygous mutant/wild-type condition of the APC gene may give rise to benign tumors, and that functional loss of this gene leads to development of tumors not only in the colon but also in other various parts of the body in FAP patients.]. 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:1351034;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP240773.RApxj5pL5h7zt7WkD4QqzLbhMT4J8ViJ5Pmte8_e8x5Lg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:57+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" .
}