@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs> .
@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:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_head {
  this: np:hasAssertion dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_assertion ;
    np:hasProvenance dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_provenance ;
    np:hasPublicationInfo dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_assertion a np:Assertion .
  dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_provenance a np:Provenance .
  dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_assertion {
  miriam-gene:3576 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_provenance {
  dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_assertion dcterms:description "[This study is aimed at 1) demonstrating the feasibility of NAF recovery from symptomatic women, 2) examining the feasibility of sequencing the entire mitochondrial genome from NAF samples, 3) cross validation of the Human mitochondrial resequencing array 2.0 (MCv2), and 4) assessing the somatic mtDNA mutation rate in benign breast diseases as a potential tool for monitoring early somatic mutations associated with 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:18402686 ;
    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 ;
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}
dgn-np:NP176384.RAH095Xu3vFAkDN-4nNRYEWZmaAS15T33mbMNivhCFjxs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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 ;
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}