@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs> .
@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:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_head {
  this: np:hasAssertion dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_assertion;
    np:hasProvenance dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_provenance;
    np:hasPublicationInfo dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_assertion a np:Assertion .
  
  dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_provenance a np:Provenance .
  
  dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_assertion {
  miriam-gene:29119 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNe39e9988a821df8e0e0e0e02c957eb5c sio:SIO_000628 miriam-gene:29119, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_provenance {
  dgn-np:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_assertion dcterms:description
      "[This study presents one of the first illustrations of successfully analyzing GWA data with a machine learning algorithm. It is shown that RF is computationally feasible for GWA data and the results obtained make biologic sense based on previous studies. More importantly, new genes were identified as potentially being associated with MS, suggesting new avenues of investigation for this complex 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:20546594;
    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:NP89013.RA91cicWbXfLXeEhgHC-kAh6wry0PL9TsMZHeeZgWZKYs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:44+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" .
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