@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA> .
@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:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_head {
  this: np:hasAssertion dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_assertion;
    np:hasProvenance dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_provenance;
    np:hasPublicationInfo dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_assertion a np:Assertion .
  
  dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_provenance a np:Provenance .
  
  dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN8ffe50c613fb13b8c13fafe6779c290b sio:SIO_000628 miriam-gene:4436, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_provenance {
  dgn-np:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_assertion dcterms:description
      "[The high frequency of microsatellite instability in lobular breast cancers, coupled with increased risk of breast cancer associated with germline mismatch repair gene mutations raises the possibility that mutations MSH2 or MLH1 might confer susceptibility to LCIS.]. 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:11369138;
    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:NP438297.RACHhA9RLkXw06umo_fvcclZUhLu2EeNqVD7s5h8s2awA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:19+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: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" .
}