@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg> .
@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:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_head {
  this: np:hasAssertion dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_assertion;
    np:hasProvenance dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_provenance;
    np:hasPublicationInfo dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_assertion a np:Assertion .
  
  dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_provenance a np:Provenance .
  
  dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGNf013e0d6103bb17a6510b817060666e9 sio:SIO_000628 miriam-gene:672, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_provenance {
  dgn-np:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_assertion dcterms:description
      "[The first 2 groups are associated with germ line mutations in the BRCA1 and BRCA2 tumor suppressor genes, whereas HNPCC is associated with germ line mutations in the DNA mismatch repair (MMR) genes, primarily hMLH1 and hMSH2.]. 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:16112002;
    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:NP176535.RAm208fs8JAvKjYNSoI2wI1E2wQPjDprGaMy2zjoVvRqg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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" .
}