@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0> .
@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:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_head {
  this: np:hasAssertion dgn-np:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_assertion ;
    np:hasProvenance dgn-np:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_provenance ;
    np:hasPublicationInfo dgn-np:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_provenance a np:Provenance .
  dgn-np:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_assertion {
  miriam-gene:19 a ncit:C16612 .
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    a sio:SIO_001121 .
}
dgn-np:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_provenance {
  dgn-np:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_assertion dcterms:description "[We present Classification by Ensembles from Random Partitions (CERP) for class prediction and apply CERP to genomic data on leukemia patients and to genomic data with several clinical variables on breast cancer patients.]. 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:17181863 ;
    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:NP688602.RAOtWXhk7QY8zy5wGVXSSFn5TJSRZFtDibLg7GKpkWld0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:58+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
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}