@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8> .
@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:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_head {
  this: np:hasAssertion dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_assertion;
    np:hasProvenance dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_provenance;
    np:hasPublicationInfo dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_assertion a np:Assertion .
  
  dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_provenance a np:Provenance .
  
  dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_assertion {
  miriam-gene:270 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGNf5ab23b9ee423aa115a69021f4a94ba5 sio:SIO_000628 miriam-gene:270, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_provenance {
  dgn-np:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_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:NP877865.RA7FJKv_02b6K1uSBWZbIyp2bu9GIm1lK9dxJX66A7lu8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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" .
}