@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc> .
@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:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_head {
  this: np:hasAssertion dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_assertion;
    np:hasProvenance dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_provenance;
    np:hasPublicationInfo dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_assertion a np:Assertion .
  
  dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_provenance a np:Provenance .
  
  dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_assertion {
  miriam-gene:7827 a ncit:C16612 .
  
  lld:C0035078 a ncit:C7057 .
  
  dgn-gda:DGN93c70756831c3db14fa6026e81e7d3e3 sio:SIO_000628 miriam-gene:7827, lld:C0035078;
    a sio:SIO_001121 .
}

dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_provenance {
  dgn-np:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_assertion dcterms:description
      "[To evaluate the incidence of posttransplant recurrence of FSGS in patients with NPHS2, the authors screened for podocin mutations in 53 patients with the clinical and pathologic stigmata of FSGS who had renal failure and who had undergone renal transplantation.Results.]. 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:12776285;
    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:NP789534.RALMNEzQ-QTboQS4JCD4pN0bHw3OFZ-eI-yVmqDhIxONc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:04+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" .
}