@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E> .
@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:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_head {
  this: np:hasAssertion dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_assertion;
    np:hasProvenance dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_provenance;
    np:hasPublicationInfo dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_assertion a np:Assertion .
  
  dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_provenance a np:Provenance .
  
  dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGN40535aca16f528c28a25a353cfa1e144 sio:SIO_000628 miriam-gene:3077, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_provenance {
  dgn-np:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_assertion dcterms:description
      "[Consistent with this, polymorphisms in the HFE gene, associated with the iron overload disorder hemochromatosis, show stronger associations with the movement disorder amyotrophic lateral sclerosis (motor neuron disease) than with cognitive impairment.]. 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:20345752;
    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:NP825785.RAZQdO71PptxzBBFwlsfkyRkP6DB9V2s9q6JjZc5T9U5E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:25+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" .
}