@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI> .
@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:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_head {
   this: np:hasAssertion dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_assertion ;
    np:hasProvenance dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_provenance ;
    np:hasPublicationInfo dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_assertion a np:Assertion .
  dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_provenance a np:Provenance .
  dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_assertion {
   miriam-gene:1356 a ncit:C16612 .
  lld:C0018995 a ncit:C7057 .
  dgn-gda:DGN4164d2e0aff8c0f50d6274f5b98f46d3 sio:SIO_000628 miriam-gene:1356 , lld:C0018995 ;
    a sio:SIO_001121 .
}
dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_provenance {
   dgn-np:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_assertion dcterms:description "[In order to investigate whether and how all these factors are interconnected, in this study we have explored the relationship of the gene variants of Hfe H63D and C282Y and of Tf C2 with serum markers of iron status (iron, ferritin, TF, TF-saturation, ceruloplasmin -CP-, CP and TF serum concentrations (CP/TF) ratio), and of liver function (albumin, transaminases, prothrombin time-prothrombin time (PT)) in a sample of 160 AD patients and 79 healthy elderly controls.]. 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:21514009 ;
    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:NP493281.RAPFr8aH8ppOGDY8yRHF0iJawu6fFNkmKEkLIGi1jFGaI130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:54+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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}