@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE> .
@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:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_head {
  this: np:hasAssertion dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_assertion;
    np:hasProvenance dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_provenance;
    np:hasPublicationInfo dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_assertion a np:Assertion .
  
  dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_provenance a np:Provenance .
  
  dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0007103 a ncit:C7057 .
  
  dgn-gda:DGNab05dd6c39d4a60e3d87271bb8e30850 sio:SIO_000628 miriam-gene:675, lld:C0007103;
    a sio:SIO_001121 .
}

dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_provenance {
  dgn-np:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_assertion dcterms:description
      "[Unselected Jewish women with EC who were diagnosed from January 1982 to January 2008 were genotyped for the predominant mutations in Jewish individuals in BRCA1 (185delAG, 5382InsC, Tyr978X) BRCA2 (6174delT), MSH2 (A636P, 324delCA) and MSH6 (c.3984_3987dup).]. 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:20850175;
    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:NP405455.RAK-kQ9lwuI5EKsOn_5klpwOh577JB5_Lz7I58HyofdkE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:01+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" .
}