@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ> .
@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:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_head {
  this: np:hasAssertion dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_assertion;
    np:hasProvenance dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_provenance;
    np:hasPublicationInfo dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_assertion a np:Assertion .
  
  dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_provenance a np:Provenance .
  
  dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_assertion {
  miriam-gene:2548 a ncit:C16612 .
  
  lld:C0016719 a ncit:C7057 .
  
  dgn-gda:DGN3593a3a688179d3dbe74ab122600f39e sio:SIO_000628 miriam-gene:2548, lld:C0016719;
    a sio:SIO_001121 .
}

dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_provenance {
  dgn-np:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_assertion dcterms:description
      "[Conventional and tissue Doppler echocardiographically derived myocardial velocity gradients (MVGs) were used to characterize the myocardium in patients with Friedreich's ataxia (FRDA), and the relationship between MVGs and the mutation in the FRDA gene, a GAA triplet repeat expansion, was investigated.]. 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:10982543;
    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:NP176371.RArCKAr2K404cSRqIxsAX-Nny9zohtUh4rxXLlJzIBMPQ130_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;
    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" .
}