@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms> .
@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:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_head {
  this: np:hasAssertion dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_assertion;
    np:hasProvenance dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_provenance;
    np:hasPublicationInfo dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_assertion a np:Assertion .
  
  dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_provenance a np:Provenance .
  
  dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN94e9f87be681d0a068e5e18ac9b1ee9f sio:SIO_000628 miriam-gene:324, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_provenance {
  dgn-np:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_assertion dcterms:description
      "[The underlying propensity for mutation at the APC gene is intriguing, while the greater frequency of mutation in cells defective for DNA repair has relevance to understanding events leading to colorectal cancer and other malignancies.]. 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:22294772;
    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:NP957688.RAMXCThBniHOVDorEz5Ts16_cqsWPjuaCo5mJCFdbKAms130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:59+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: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" .
}