@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM> .
@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:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_head {
  this: np:hasAssertion dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_assertion;
    np:hasProvenance dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_provenance;
    np:hasPublicationInfo dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_assertion a np:Assertion .
  
  dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_provenance a np:Provenance .
  
  dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_assertion {
  miriam-gene:81 a ncit:C16612 .
  
  lld:C0035078 a ncit:C7057 .
  
  dgn-gda:DGN134a27e6089849155a32bd405606e433 sio:SIO_000628 miriam-gene:81, lld:C0035078;
    a sio:SIO_001121 .
}

dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_provenance {
  dgn-np:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_assertion dcterms:description
      "[A variation in the MYH9 locus of chromosome 22 has been associated with increased risk for idiopathic FSGS, hypertensive nephrosclerosis and HIVAN and may explain much of the increased risks of ESRD and FSGS among African-Americans.]. 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:20979964;
    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:NP848969.RAMyVi2uhh7PmMvbPQGskA6DUt3ZtVOkjxRXJbAuhGrBM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:39+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" .
}