@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs> .
@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:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_head {
  this: np:hasAssertion dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_assertion;
    np:hasProvenance dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_provenance;
    np:hasPublicationInfo dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_assertion a np:Assertion .
  
  dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_provenance a np:Provenance .
  
  dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_assertion {
  miriam-gene:1436 a ncit:C16612 .
  
  lld:C0085669 a ncit:C7057 .
  
  dgn-gda:DGN24f7031b1d7c858d7960ec8d06e534ee sio:SIO_000628 miriam-gene:1436, lld:C0085669;
    a sio:SIO_001121 .
}

dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_provenance {
  dgn-np:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_assertion dcterms:description
      "[A cohort of 75 MDS patients were investigated for RAS, FMS and p53 mutations, and these molecular findings were related to cytogenetics, clinical status, transformation to acute leukemia, prognostic scores and survival.]. 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:9639416;
    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:NP195395.RAENrQ4kvtUSZ1RkNnExxjFnYEjnB70cMLvwIdhrdEXhs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:47+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" .
}