@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU> .
@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:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_head {
  this: np:hasAssertion dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_assertion;
    np:hasProvenance dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_provenance;
    np:hasPublicationInfo dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_assertion a np:Assertion .
  
  dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_provenance a np:Provenance .
  
  dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_assertion {
  miriam-gene:5245 a ncit:C16612 .
  
  lld:C0346153 a ncit:C7057 .
  
  dgn-gda:DGNc617e15b7e3e87f2a40cd96d20df1765 sio:SIO_000628 miriam-gene:5245, lld:C0346153;
    a sio:SIO_001121 .
}

dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_provenance {
  dgn-np:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_assertion dcterms:description
      "[The C to T transition in the 3' untranslated region of the prohibitin (PHB) gene alters mRNA function and has recently been shown to be associated with hereditary breast cancer risk in Polish women harbouring BRCA1 mutations.]. 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:18397521;
    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:NP426303.RA9O77bynjql_tC9TYWxf9HQbtTnaQYnZHdmb12faRbwU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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" .
}