@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU> .
@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:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_head {
  this: np:hasAssertion dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_assertion;
    np:hasProvenance dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_provenance;
    np:hasPublicationInfo dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_assertion a np:Assertion .
  
  dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_provenance a np:Provenance .
  
  dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C0007103 a ncit:C7057 .
  
  dgn-gda:DGN2faf450c68cfc796150f73bbade6a8cd sio:SIO_000628 miriam-gene:4436, lld:C0007103;
    a sio:SIO_001121 .
}

dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_provenance {
  dgn-np:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_assertion dcterms:description
      "[In the United States, it was recently reported that the prevalence of Lynch syndrome with an hMSH2 mutation in patients with endometrial cancer in the lower uterine segment (LUS) is much greater than that in patients with endometrial cancer, although no such reports have been published in Asia.]. 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:22940821;
    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:NP569705.RASnm68W9egVm7aOR_rFergifRCH58lu9m4lWpQiqmAHU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:19+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" .
}