@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE> .
@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:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_head {
  this: np:hasAssertion dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_assertion;
    np:hasProvenance dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_provenance;
    np:hasPublicationInfo dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_assertion a np:Assertion .
  
  dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_provenance a np:Provenance .
  
  dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN10df39742d3cd0b1a5548e5eb1289bd7 sio:SIO_000628 miriam-gene:3077, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_provenance {
  dgn-np:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_assertion dcterms:description
      "[HFE participates in the regulation of iron metabolism, its mutations are primary cause of hereditary hemochromatosis and appear to be more frequent in neurodegenerative disorders such as Alzheimer's disease and amyotrophic lateral sclerosis.]. 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:18325820;
    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:NP433666.RAUIXbViFkcLSugPt1NLQtEbFwwGqBE_QCKwaknYcAPsE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:17+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>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}