@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY> .
@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/v3.0.0/void/> .

dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_head {
  this: np:hasAssertion dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_assertion;
    np:hasProvenance dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_provenance;
    np:hasPublicationInfo dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_assertion a np:Assertion .
  
  dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_provenance a np:Provenance .
  
  dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  
  lld:C1458156 a ncit:C7057 .
  
  dgn-gda:DGN37429a10f141d4fb7b10f1ebe538369f sio:SIO_000628 miriam-gene:3075, lld:C1458156;
    a sio:SIO_001121 .
}

dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_provenance {
  dgn-np:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_assertion dcterms:description
      "[The absence of a more severe CFH genotype assisted in the decision for retransplantation and suggests the importance of genetic mutation screening in order to stratify the risk of disease recurrence and graft loss versus the benefit of transplantation.]. 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:24671321;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP446576.RAOMn0jcaAqxdwX8dj2GxbMrMAVsC9NSJwgokfhJuSqyY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:01+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}