@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU> .
@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:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_head {
  this: np:hasAssertion dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_assertion;
    np:hasProvenance dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_provenance;
    np:hasPublicationInfo dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_assertion a np:Assertion .
  
  dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_provenance a np:Provenance .
  
  dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_assertion {
  miriam-gene:1630 a ncit:C16612 .
  
  lld:C0007102 a ncit:C7057 .
  
  dgn-gda:DGNb8b7810c0b7c06e8ab8844bba6c716de sio:SIO_000628 miriam-gene:1630, lld:C0007102;
    a sio:SIO_001121 .
}

dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_provenance {
  dgn-np:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_assertion dcterms:description
      "[Because both ovarian and colon cancer are features of Lynch syndrome II, which has been provisionally mapped to chromosome 18, we hypothesized that loss of heterozygosity at the DCC locus may also occur in ovarian neoplasia.]. 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:1594239;
    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:NP504224.RAEnm8sOho7AW-iCQcxjILfiOZfk1gMpwMGQ4kL1C4wBU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:00+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" .
}