@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo> .
@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:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_head {
  this: np:hasAssertion dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_assertion ;
    np:hasProvenance dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_provenance ;
    np:hasPublicationInfo dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_assertion a np:Assertion .
  dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_provenance a np:Provenance .
  dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_assertion {
  miriam-gene:10878 a ncit:C16612 .
  lld:C0034155 a ncit:C7057 .
  dgn-gda:DGN7278b2b8d0e7f5fc8250ed2cf76588c7 sio:SIO_000628 miriam-gene:10878 , lld:C0034155 ;
    a sio:SIO_001121 .
}
dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_provenance {
  dgn-np:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_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:NP818478.RAdr5OI8T0K6BSMc_txqU3jOcPUytBzr1xVGGEOn_cplo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:21+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" .
}