@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A> .
@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 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:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_head {
  this: np:hasAssertion dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_assertion;
    np:hasProvenance dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_provenance;
    np:hasPublicationInfo dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_assertion a np:Assertion .
  
  dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_provenance a np:Provenance .
  
  dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0027831 a ncit:C7057 .
  
  dgn-gda:DGNc7423db5b81cf7ded08ca201c4475509 sio:SIO_000628 miriam-gene:4360, lld:C0027831;
    a sio:SIO_001121 .
}

dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_provenance {
  dgn-np:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_assertion dc:description
      "[Nevertheless, the observation of frequent alterations of key growth regulatory genes in MMR-deficient cells such as NF1, APC, p53, K-Ras, with no significant excess of frameshift mutations and changes at short coding repeats, suggest that even in the presence of an inherited tendency to genomic instability, tumor progression is mainly driven by a process of natural selection.]. 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:16528606;
    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:NP379607.RABgiPAYPLG2PHiiR9masuAGTsBghsNBMpVdYu7x86o3A130_publicationInfo {
  this: dc:created "2014-10-02T12:35:44+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}