@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4> .
@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/v4.0.0/void/> .
dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_head {
   this: np:hasAssertion dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_assertion ;
    np:hasProvenance dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_provenance ;
    np:hasPublicationInfo dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_assertion a np:Assertion .
  dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_provenance a np:Provenance .
  dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_assertion {
   miriam-gene:3077 a ncit:C16612 .
  lld:C0524910 a ncit:C7057 .
  dgn-gda:DGN7ecfc9a4fa4e0ffc53df6b84106271dd sio:SIO_000628 miriam-gene:3077 , lld:C0524910 ;
    a sio:SIO_001121 .
}
dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_provenance {
   dgn-np:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_assertion dcterms:description "[The presence of HFE mutations is independently associated with iron loading and advanced fibrosis in patients with compensated liver disease from chronic hepatitis C, especially after controlling for duration of disease.]. 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:12557137 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP382106.RAsshW6rp4EPu2zUIFafGh9Rn3XlU19bNTHstybNNM9t4130_publicationInfo {
   this: dcterms:created "2016-05-13T12:44:38+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}