@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_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:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_head {
   this: np:hasAssertion dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_assertion ;
    np:hasProvenance dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_provenance ;
    np:hasPublicationInfo dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_assertion a np:Assertion .
  dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_provenance a np:Provenance .
  dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_assertion {
   miriam-gene:81494 a ncit:C16612 .
  lld:C0026821 a ncit:C7057 .
  dgn-gda:DGN02425b96fad8b00292e7730ada4d97a9 sio:SIO_000628 miriam-gene:81494 , lld:C0026821 ;
    a sio:SIO_001121 .
}
dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_provenance {
   dgn-np:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_assertion dcterms:description "[In this review, these and other diseases, which often present with isolated microscopic hematuria, including hereditary angiopathy, nephropathy, aneurysms, and muscle cramps (HANAC) syndrome, IgA nephropathy, and CFHR5 nephropathy, are discussed together with the associated molecular pathology, clinical features, and prognosis.]. 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:23325022 ;
    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:NP484272.RA8IpwDoySB4jdp7w5ixH-Ol563GyVm7WiVRcWpUB2f_E130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:49+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" .
}