@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10> .
@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:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_head {
   this: np:hasAssertion dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_assertion ;
    np:hasProvenance dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_provenance ;
    np:hasPublicationInfo dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_assertion a np:Assertion .
  dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_provenance a np:Provenance .
  dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_assertion {
   miriam-gene:4084 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGNdb485cf2d8a996a9224290f182d2ae11 sio:SIO_000628 miriam-gene:4084 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_provenance {
   dgn-np:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_assertion dcterms:description "[We have previously shown that expression changes of the mitotic arrest deficiency (MAD) gene family plays a role in renal cell cancer (RCC) characterized by numerical chromosomal changes, namely papillary and chromophobe carcinomas, but nothing is known about the expression of mitotic checkpoint genes in the clear cell histotype (ccRCC).]. 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:18791270 ;
    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:NP283743.RAx15i0H6CrawH38rDNGRD51QZFKSE7M83YfKknyLkE10130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:40+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" .
}