@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U> .
@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:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_head {
  this: np:hasAssertion dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_assertion;
    np:hasProvenance dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_provenance;
    np:hasPublicationInfo dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_assertion a np:Assertion .
  
  dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_provenance a np:Provenance .
  
  dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0741237 a ncit:C7057 .
  
  dgn-gda:DGN284993821cb405cb22c85f82797c1ce2 sio:SIO_000628 miriam-gene:3077, lld:C0741237;
    a sio:SIO_001121 .
}

dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_provenance {
  dgn-np:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_assertion dcterms:description
      "[More detailed study of arthritis symptoms and signs over time in individuals with and without mutations in the HFE gene is necessary to determine the contribution of HFE genes to arthritis in the population.]. 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:14673391;
    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:NP225479.RABF9-uDUUcnFUr-Fu0mF5P97mnGZCR1kH4un0v4_sy7U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:05+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" .
}