@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM> .
@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:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_head {
  this: np:hasAssertion dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_assertion;
    np:hasProvenance dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_provenance;
    np:hasPublicationInfo dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_assertion a np:Assertion .
  
  dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_provenance a np:Provenance .
  
  dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGN4fde35a4070b86db128e349fcc7b5fb8 sio:SIO_000628 miriam-gene:675, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_provenance {
  dgn-np:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_assertion dcterms:description
      "[These data suggest that mutations of BRCA2 are rare in sporadic ovarian cancers, and that the proportion of ovarian cancers resulting from hereditary predisposition may be higher than previously suspected based on estimates derived from studies of highly penetrant genetic loci.]. 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:8665505;
    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:NP1351908.RAI8IOdKyaAvxD4FysKtshbs6FzgO_RSqsrTeO_T-1cgM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:59+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" .
}