@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U> .
@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:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_head {
  this: np:hasAssertion dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_assertion;
    np:hasProvenance dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_provenance;
    np:hasPublicationInfo dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_assertion a np:Assertion .
  
  dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_provenance a np:Provenance .
  
  dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_assertion {
  miriam-gene:4627 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN1d2753a251ea7c43ba83801bcd13d811 sio:SIO_000628 miriam-gene:4627, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_provenance {
  dgn-np:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_assertion dcterms:description
      "[These new data demonstrate that much of the excess risk of ESRD in African American individuals is attributable to an MYH9 risk haplotype and suggest that hypertension may cause progressive kidney disease only in genetically susceptible individuals or be the result of a primary renal disease.]. 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:18923054;
    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:NP233155.RANIoSoolaaWlrnAY-1HlYP6rtQgiH_GidT4hattzyK6U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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" .
}