@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE> .
@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/v3.0.0/void/> .

dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_head {
  this: np:hasAssertion dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_assertion;
    np:hasProvenance dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_provenance;
    np:hasPublicationInfo dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_assertion a np:Assertion .
  
  dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_provenance a np:Provenance .
  
  dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_assertion {
  miriam-gene:4548 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN24da6721c779d8812c903dc918ce0f45 sio:SIO_000628 miriam-gene:4548, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_provenance {
  dgn-np:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_assertion dcterms:description
      "[The role of allele variants 677T and 1298C (MTHFR gene) and 2756G (MS gene) has been investigated as potentially modifying factors of BRCA gene penetrance, evaluated as age at first diagnosis of cancer, in 484 BRCA1/BRCA2 carriers and in 108 sporadic breast cancer cases as a control group.]. 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:17151928;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP577201.RArDRXw0sefvF86nmTg0S8wMOGHHiglW7DrzP6YR8IPVE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:23+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}