@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_head {
  this: np:hasAssertion dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_assertion;
    np:hasProvenance dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_provenance;
    np:hasPublicationInfo dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_assertion a np:Assertion .
  
  dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_provenance a np:Provenance .
  
  dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_assertion {
  miriam-gene:1287 a ncit:C16612 .
  
  lld:C1567741 a ncit:C7057 .
  
  dgn-gda:DGNb72951239a29dfb7f88a3a57e5ad86e6 sio:SIO_000628 miriam-gene:1287, lld:C1567741;
    a sio:SIO_001121 .
}

dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_provenance {
  dgn-np:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_assertion dcterms:description
      "[The results indicate that mutations in COL4A5 that leading to renal failure are more frequent than those involved in classic Alport syndrome, and also that mutations in COL4A6 are not likely to cause this disease.]. 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:8738805;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1354756.RAXweAzp1EgguYSCZWAQUqsFbOvUD1RqhfAajBUeDxjlg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:00+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}