@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4> .
@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:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_head {
  this: np:hasAssertion dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_assertion;
    np:hasProvenance dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_provenance;
    np:hasPublicationInfo dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_assertion a np:Assertion .
  
  dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_provenance a np:Provenance .
  
  dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C0007103 a ncit:C7057 .
  
  dgn-gda:DGN232bd69c190ba38d3edd0b6da2cfacf9 sio:SIO_000628 miriam-gene:4436, lld:C0007103;
    a sio:SIO_001122 .
}

dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_provenance {
  dgn-np:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_assertion dcterms:description
      "[Genetic counseling and testing for the MSH2 A636P mutation is indicated for Ashkenazi Jewish women with an endometrial cancer, especially if the cancer is detected before the age of 70 years in women with a personal or family history of colorectal cancer.]. 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:18674656;
    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:NP685606.RAw-kVwn4zDKhO63T91bhJRBPGhPTsZJxAYCEhZNMHlr4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:56+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" .
}