@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A> .
@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:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_head {
  this: np:hasAssertion dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_assertion;
    np:hasProvenance dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_provenance;
    np:hasPublicationInfo dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_assertion a np:Assertion .
  
  dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_provenance a np:Provenance .
  
  dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGNfb3224ad816e29e57c757494f161d553 sio:SIO_000628 miriam-gene:3077, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_provenance {
  dgn-np:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_assertion dcterms:description
      "[We examined four known polymorphisms, C282Y and H63D in the HFE gene, G258S in the TF gene and S82G in the TFR gene, in 181 sporadic PD patients and 180 controls from Southern Italy to investigate their possible role in susceptibility to PD.]. 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:21384276;
    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:NP608857.RAHgwrWo2CaJyhjMBbd16ALjIZLb67KSemF-9_RbhWm5A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:05+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" .
}