@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8> .
@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:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_head {
  this: np:hasAssertion dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_assertion;
    np:hasProvenance dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_provenance;
    np:hasPublicationInfo dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_assertion a np:Assertion .
  
  dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_provenance a np:Provenance .
  
  dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN0c00633166a5632324ffe44450b20901 sio:SIO_000628 miriam-gene:675, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_provenance {
  dgn-np:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_assertion dcterms:description
      "[From these data, one can estimate the penetrance of an autosomal dominant gene, and this technique has been used to estimate the probability that Ashkenazi Jewish women with specific mutations of BRCA1 or BRCA2 will develop breast cancer.]. 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:10854487;
    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:NP157553.RAfLx3K0SotlKTI-JF6QYxo8oyXELzW7LTpSB83L8RSu8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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" .
}