@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk> .
@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:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_head {
  this: np:hasAssertion dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_assertion ;
    np:hasProvenance dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_provenance ;
    np:hasPublicationInfo dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_assertion a np:Assertion .
  dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_provenance a np:Provenance .
  dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  lld:C0409959 a ncit:C7057 .
  dgn-gda:DGN0b9b0008c990ba2812df0e1fc2849e0a sio:SIO_000628 miriam-gene:3077 , lld:C0409959 ;
    a sio:SIO_001122 .
}
dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_provenance {
  dgn-np:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_assertion dcterms:description "[A predicted difference in SF ferritin concentrations in patients with knee OA was confirmed. Concentrations of ferritin in the SF were found to be two- to threefold higher in knee OA patients with HFE gene mutations compared to wt patients. This finding is consistent with the possibility that, in OA patients with HFE gene mutations, localized iron overload may contribute either directly or indirectly to osteochondral damage, possibly in a similar way to that which occurs in the arthropathy that complicates HH.]. 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:20560808 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP86845.RAbM8bEF59Afjw7WYmmuGhr_sBgzl5MsvEdRjNOsUaHrk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+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> ;
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    pav:version "v2.1.0.0" .
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}