@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU> .
@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/v4.0.0/void/> .
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_head {
  this: np:hasAssertion dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion ;
    np:hasProvenance dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance ;
    np:hasPublicationInfo dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion a np:Assertion .
  dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance a np:Provenance .
  dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion {
  miriam-gene:213 a ncit:C16612 .
  lld:C0022658 a ncit:C7057 .
  dgn-gda:DGNf3b63273b3cc0cb5a84d49add2ddf861 sio:SIO_000628 miriam-gene:213 , lld:C0022658 ;
    a sio:SIO_001121 .
}
dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance {
  dgn-np:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion dcterms:description "[Four single nucleotide polymorphisms comprising the major MYH9 E1 risk haplotype were tested for association with estimated glomerular filtration rate (eGFR) and urine albumin:creatinine ratio (ACR) in 2,903 HyperGEN participants (1,458 African Americans (AA) in 895 families and 1,445 European Americans (EA) in 859 families) to determine the role of MYH9 in subclinical 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:19153477 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:09+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}