@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E> .
@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:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_head {
  this: np:hasAssertion dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_assertion ;
    np:hasProvenance dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_provenance ;
    np:hasPublicationInfo dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_assertion a np:Assertion .
  dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_provenance a np:Provenance .
  dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_assertion {
  miriam-gene:4868 a ncit:C16612 .
  lld:C0022658 a ncit:C7057 .
  dgn-gda:DGN35290192bf629f4be9383b0710a04c56 sio:SIO_000628 miriam-gene:4868 , lld:C0022658 ;
    a sio:SIO_001121 .
}
dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_provenance {
  dgn-np:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_assertion dcterms:description "[Mutations affecting a number of slit diaphragm proteins, including nephrin (encoded by NPHS1), lead to renal disease owing to disruption of the filtration barrier and rearrangement of the actin cytoskeleton, although the molecular basis for this is unclear.]. 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:16525419 ;
    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:NP539253.RA7AHDWZCePpIfXIJG2i79h72k81867zCW3lahX6wDO7E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:49+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" .
}