@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4> .
@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:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_head {
  this: np:hasAssertion dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_assertion;
    np:hasProvenance dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_provenance;
    np:hasPublicationInfo dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_assertion a np:Assertion .
  
  dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_provenance a np:Provenance .
  
  dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN3c0560f4135cff273467c77f87f1fc24 sio:SIO_000628 miriam-gene:4292, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_provenance {
  dgn-np:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_assertion dcterms:description
      "[To determine the validity of observations suggesting a significant dichotomy of gynecologic cancers determined by linkage to specific genetic defects associated with two major autosomal dominant hereditary cancer syndromes; the Creighton University Hereditary Cancer Registry was searched for female carriers of germ line mutations in BRCA1 and BRCA2, associated with the Hereditary Breast Ovarian Cancer syndrome, and in the mismatch repair (MMR) genes MLH1, MSH2 and MSH6, associated with Lynch syndrome, who were registered with invasive uterine, ovarian, fallopian tube or peritoneal cancers between January 1, 1959 and December 31, 2010.]. 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:23666231;
    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:NP1077010.RAPc0YHFcQPoosUtj0324GTXVn85I1iTltLh_7ncLKHg4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:54+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" .
}