@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk> .
@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/v3.0.0/void/> .

dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_head {
  this: np:hasAssertion dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_assertion;
    np:hasProvenance dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_provenance;
    np:hasPublicationInfo dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_assertion a np:Assertion .
  
  dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_provenance a np:Provenance .
  
  dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_assertion {
  miriam-gene:7225 a ncit:C16612 .
  
  lld:C2919166 a ncit:C7057 .
  
  dgn-gda:DGNfbc3f1b31f5dc2ec80e6e41e5c4ada0b sio:SIO_000628 miriam-gene:7225, lld:C2919166;
    a sio:SIO_001121 .
}

dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_provenance {
  dgn-np:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_assertion dcterms:description
      "[Gain-of-function mutations in the calcium channel TRPC6 lead to autosomal dominant focal segmental glomerulosclerosis and podocyte expression of TRPC6 is increased in some acquired human glomerular diseases, particularly in membranous nephropathy.]. 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:24194522;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP758410.RAXOyuaUP0fClmpsL8H0WBamkygczk8h7J5FscJeAUozk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:17+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}