@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw> .
@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:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_head {
  this: np:hasAssertion dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_assertion;
    np:hasProvenance dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_provenance;
    np:hasPublicationInfo dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_assertion a np:Assertion .
  
  dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_provenance a np:Provenance .
  
  dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_assertion {
  miriam-gene:4627 a ncit:C16612 .
  
  lld:C0022661 a ncit:C7057 .
  
  dgn-gda:DGN0476f628ad50f70775afa2baf5959d50 sio:SIO_000628 miriam-gene:4627, lld:C0022661;
    a sio:SIO_001121 .
}

dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_provenance {
  dgn-np:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_assertion dcterms:description
      "[This led us to re-examine the interval surrounding MYH9 and to the detection of novel missense mutations with predicted functional effects in the neighboring APOL1 gene, which are significantly more associated with ESKD than all previously reported SNPs in MYH9.]. 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:20635188;
    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:NP343648.RADTIBtFOeTVmXzxhLhn-oCuFq2gn3oNDX-zcBETXLitw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:22+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" .
}