@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw> .
@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:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_head {
  this: np:hasAssertion dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_assertion;
    np:hasProvenance dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_provenance;
    np:hasPublicationInfo dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_assertion a np:Assertion .
  
  dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_provenance a np:Provenance .
  
  dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_assertion {
  miriam-gene:27130 a ncit:C16612 .
  
  lld:C0020258 a ncit:C7057 .
  
  dgn-gda:DGN176ea7d428d92fff20b59f580254471d sio:SIO_000628 miriam-gene:27130, lld:C0020258;
    a sio:SIO_001121 .
}

dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_provenance {
  dgn-np:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_assertion dcterms:description
      "[Positional cloning and candidate gene approaches led to the identification of eight causative genes (NPHP1, 3, 4, 5, 6, 7, 8, and 9) responsible for the juvenile NPH and one gene NPHP2 for the infantile form.]. 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:18607645;
    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:NP367976.RAVaSHwsFuJ23TIh79_fnHNefuztkRIG5EeXNT0bqriEw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:35+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" .
}