@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M> .
@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 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:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_head {
  this: np:hasAssertion dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_assertion;
    np:hasProvenance dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_provenance;
    np:hasPublicationInfo dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_assertion a np:Assertion .
  
  dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_provenance a np:Provenance .
  
  dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_assertion {
  miriam-gene:81 a ncit:C16612 .
  
  lld:C0017668 a ncit:C7057 .
  
  dgn-gda:DGN8fa57b9d37ba22f88bfd649147cb55b5 sio:SIO_000628 miriam-gene:81, lld:C0017668;
    a sio:SIO_001121 .
}

dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_provenance {
  dgn-np:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_assertion dc:description
      "[To investigate the promoter mutations of ACTN4 and SYNPO genes in patients with idiopathic focal segmental glomerulosclerosis (FSGS), and to provide functional analysis of these mutations in the role of FSGS occurrence.]. 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:19666657;
    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:NP381628.RABoAL3Bbc-mCrR_lsfVkFZl0AuuxuxOKMuq_cszBTS0M130_publicationInfo {
  this: dc:created "2014-10-02T12:35:45+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}