@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E> .
@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:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_head {
  this: np:hasAssertion dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion;
    np:hasProvenance dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance;
    np:hasPublicationInfo dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion a np:Assertion .
  
  dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance a np:Provenance .
  
  dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion {
  miriam-gene:4620 a ncit:C16612 .
  
  lld:C1561643 a ncit:C7057 .
  
  dgn-gda:DGN959de879afaa397b97100eb4fb4cae73 sio:SIO_000628 miriam-gene:4620, lld:C1561643;
    a sio:SIO_001121 .
}

dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance {
  dgn-np:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion dcterms:description
      "[MYH9-related disorders are rare causes of chronic kidney disease (CKD) presenting as chronic glomerulonephritis and derive from mutations of the MYH9 gene, which encodes for the nonmuscle myosin heavy chain IIA.]. 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:19726116;
    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:NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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: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" .
}