@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s> .
@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:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_head {
  this: np:hasAssertion dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_assertion;
    np:hasProvenance dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_provenance;
    np:hasPublicationInfo dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_assertion a np:Assertion .
  
  dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_provenance a np:Provenance .
  
  dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGNfb34a8cee6bd993f65ba972bfbc2361a sio:SIO_000628 miriam-gene:3077, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_provenance {
  dgn-np:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_assertion dcterms:description
      "[HFE-related genetic haemochromatosis (GH) is the commonest inherited genetic disorder in Caucasian populations with approximately one in 180 of individuals in the west of Scotland homozygous for the common C282Y mutation.]. 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:18403938;
    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:NP217007.RAzVbUT9h_YC6HlEg1G2lY2ZEATKjf7fFKM5rqKqeHG5s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}