@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY> .
@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:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_head {
  this: np:hasAssertion dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_assertion;
    np:hasProvenance dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_provenance;
    np:hasPublicationInfo dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_assertion a np:Assertion .
  
  dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_provenance a np:Provenance .
  
  dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_assertion {
  miriam-gene:23417 a ncit:C16612 .
  
  lld:C2939174 a ncit:C7057 .
  
  dgn-gda:DGN6054d3065a4786cc011dfe87f3b6c4d7 sio:SIO_000628 miriam-gene:23417, lld:C2939174;
    a sio:SIO_001121 .
}

dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_provenance {
  dgn-np:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_assertion dcterms:description
      "[There is a group of inherited cystic nephropathies that are characterized by juvenile onset recessive inheritance (familial juvenile nephronophthisis, FJN) or by adult onset dominant inheritance (medullary cystic disease, MCD) and share similar clinico-pathological presentation to the extent that they are usually grouped together under the term FJN/MCD complex.]. 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:9536096;
    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:NP263905.RAYnlxxm3jWAtBTrIrD9do6xTQ2MWrxhEbx6iYDPtbgvY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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" .
}