@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w> .
@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:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_head {
  this: np:hasAssertion dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion;
    np:hasProvenance dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance;
    np:hasPublicationInfo dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion a np:Assertion .
  
  dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance a np:Provenance .
  
  dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
  dgn-gda:DGN74ddcb2b2f499aac51401bfc57f1c231 sio:SIO_000628 miriam-gene:3075, lld:C0022658;
    a sio:SIO_001121 .
}

dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance {
  dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion dcterms:description
      "[Mutations in the Factor H gene are associated with severe and diverse diseases including the rare renal disorders hemolytic uremic syndrome (HUS) and membranoproliferative glomerulonephritis (MPGN) also termed dense deposit disease (DDD), as well as the more frequent retinal disease age related macular degeneration (AMD).]. 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:19388168;
    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:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:55+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" .
}