@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw> .
@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:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_head {
  this: np:hasAssertion dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_assertion;
    np:hasProvenance dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_provenance;
    np:hasPublicationInfo dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_assertion a np:Assertion .
  
  dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_provenance a np:Provenance .
  
  dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN2d81b4226a8d0ba52cd75ec87939c3fa sio:SIO_000628 miriam-gene:4524, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_provenance {
  dgn-np:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_assertion dcterms:description
      "[Clinical (sex, age, type of MS, relapse, disease duration, coexisting disease, smoking habit, and physical disability) and laboratory variables (HHcy, low serum levels of folate and vit.B12, MTHFR genotype) were evaluated for their ability to predict 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:18080853;
    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:NP69518.RAYyGIV-4CSvOuf-QFlOPjSyETJ5GjoeUA8Uf0V09F1fw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:33+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" .
}