@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I> .
@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:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_head {
  this: np:hasAssertion dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_assertion;
    np:hasProvenance dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_provenance;
    np:hasPublicationInfo dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_assertion a np:Assertion .
  
  dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_provenance a np:Provenance .
  
  dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGNbca9c215240cb699f3b9457ba3d39712 sio:SIO_000628 miriam-gene:324, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_provenance {
  dgn-np:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_assertion dcterms:description
      "[Molecular testing directed at colorectal neoplasia is currently in use for diagnosis and characterization of rare, highly penetrant inherited syndromes due to germline mutation of the APC suppressor gene or DNA nucleotide mismatch repair genes.]. 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:10539901;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP215545.RAdtP9bMBkvwOdmu3s_j-KLDvROO7naGQWRiTVTC2659I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:59+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" .
}