@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4> .
@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:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_head {
   this: np:hasAssertion dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_assertion ;
    np:hasProvenance dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_provenance ;
    np:hasPublicationInfo dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_assertion a np:Assertion .
  dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_provenance a np:Provenance .
  dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_assertion {
   miriam-gene:5245 a ncit:C16612 .
  lld:C0029925 a ncit:C7057 .
  dgn-gda:DGN8556d56351d20b361b7b66012e7ff542 sio:SIO_000628 miriam-gene:5245 , lld:C0029925 ;
    a sio:SIO_001121 .
}
dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_provenance {
   dgn-np:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_assertion dcterms:description "[To evaluate the potential role of genetic variants within PHB and MTHFR in breast and ovarian cancer risk, 4102 BRCA1 and 2093 BRCA2 mutation carriers, and 6211 BRCA1 and 2902 BRCA2 carriers from the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA) were genotyped for the PHB 1630 C>T (rs6917) polymorphism and the MTHFR 677 C>T (rs1801133) polymorphism, respectively.]. 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:22669161 ;
    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:NP395012.RAB0g-eZN0iAuJjNSSIqKTMz2cnFFpEUPnfTk5mk8dxK4130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:55+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" .
}