@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA> .
@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/v3.0.0/void/> .

dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_head {
  this: np:hasAssertion dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_assertion;
    np:hasProvenance dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_provenance;
    np:hasPublicationInfo dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_assertion a np:Assertion .
  
  dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_provenance a np:Provenance .
  
  dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C3495559 a ncit:C7057 .
  
  dgn-gda:DGNbec368b3d72f96d1e931ea00be3b6a26 sio:SIO_000628 miriam-gene:3077, lld:C3495559;
    a sio:SIO_001122 .
}

dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_provenance {
  dgn-np:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_assertion dcterms:description
      "[In 32 patients with hereditary hemochromatosis, in 84 patients with polymyositis or dermatomyositis, in 246 patients with juvenile idiopathic arthritis and in 481 persons of the control group the presence of HFE gene mutations was etablished.]. 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:16047841;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP50129.RAzFgYtrmH6-czMeU3s8vBKYBTKkYDe7u83uo4Y4W2dkA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:07+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}