@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4> .
@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:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_head {
  this: np:hasAssertion dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_assertion ;
    np:hasProvenance dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_provenance ;
    np:hasPublicationInfo dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_assertion a np:Assertion .
  dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_provenance a np:Provenance .
  dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_assertion {
  miriam-gene:3078 a ncit:C16612 .
  lld:C0034155 a ncit:C7057 .
  dgn-gda:DGN6b81e8b0d4fadb24797678fa039c675c sio:SIO_000628 miriam-gene:3078 , lld:C0034155 ;
    a sio:SIO_001121 .
}
dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_provenance {
  dgn-np:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_assertion dcterms:description "[In TTP against ADAMTS 13, the vWF cleaving protease and in the DEAP-HUS (Deficient for CFHR1 and CFHR3 proteins and autoantibody positive) group against the major complement regulator Factor H. Autoantibodies in MPGN are termed C3 Nephritic Factor (C3NeF) and are directed against a neoepitope of the complement C3 convertase C3bBb.]. 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:19640589 ;
    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:NP566127.RA7mv3DJD5wFnm5fGvEAFgNL0e1lChNtGYc7Ra88mAEK4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:41+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" .
}