@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU> .
@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:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_head {
  this: np:hasAssertion dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_assertion;
    np:hasProvenance dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_provenance;
    np:hasPublicationInfo dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_assertion a np:Assertion .
  
  dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_provenance a np:Provenance .
  
  dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN6d2f50853e91b5595216a07bfebcf00e sio:SIO_000628 miriam-gene:3077, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_provenance {
  dgn-np:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_assertion dcterms:description
      "[in the Italian population, the most common HFE mutations, H63D and C282Y are not associated with the individual risk to develop PD, nor have specific influence on the clinical features of the disease.]. 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:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP42612.RALFa7jW9S7OmePgWBUVu-3P7toyaisYG3QXLJUG0-5dU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:19+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" .
}