@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM> .
@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:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_head {
  this: np:hasAssertion dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_assertion ;
    np:hasProvenance dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_provenance ;
    np:hasPublicationInfo dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_assertion a np:Assertion .
  dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_provenance a np:Provenance .
  dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  lld:C0162309 a ncit:C7057 .
  dgn-gda:DGN501d6be6aedeaccc17be575e2295cc5f sio:SIO_000628 miriam-gene:3077 , lld:C0162309 ;
    a sio:SIO_001121 .
}
dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_provenance {
  dgn-np:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_assertion dcterms:description "[The aim of the study was to determine the prevalence of C282Y and H63D mutations in patients with ALD and healthy individuals and to analyze laboratory data in the context of HFE gene mutation in ALD patients.]. 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:20424537 ;
    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:NP519208.RAdEnVCzmm6iXRWgUFXPbxpVWVniSNP60aS191ObDDZQM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:09+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> ;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
}