@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI> .
@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:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_head {
  this: np:hasAssertion dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_assertion;
    np:hasProvenance dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_provenance;
    np:hasPublicationInfo dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_assertion a np:Assertion .
  
  dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_provenance a np:Provenance .
  
  dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1512981 a ncit:C7057 .
  
  dgn-gda:DGN7aa5b7f77901665063536bd81464490f sio:SIO_000628 miriam-gene:672, lld:C1512981;
    a sio:SIO_001121 .
}

dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_provenance {
  dgn-np:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_assertion dcterms:description
      "[Our results, indicating that missense mutations of BRCA1 and BRCA2 tend to predominate over frameshifts or nonsense mutations in Japanese breast cancer families, will contribute significantly to an understanding of mammary tumorigenesis in Japan, and will be of vital importance for future genetic testing.]. 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:9609997;
    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:NP303010.RAGAriLHNGqpen1ZuDjmHP7sitAiiI9nEVvD9nfXhvIxI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:54+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" .
}