@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI> .
@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:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_head {
  this: np:hasAssertion dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_assertion;
    np:hasProvenance dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_provenance;
    np:hasPublicationInfo dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_assertion a np:Assertion .
  
  dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_provenance a np:Provenance .
  
  dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGN1f315cf4d5e18f8ee707334f616fed19 sio:SIO_000628 miriam-gene:2272, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_provenance {
  dgn-np:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_assertion dcterms:description
      "[These results suggested that aberrant methylation of the FHIT gene might be one of molecular events involved in the disease progression of MDS and be an adverse prognostic factor in MDS.]. 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:18367246;
    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:NP653446.RAacS-p2M_l1e2YBGpSdMAF_4njuevMCwfhZ19rOATNfI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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" .
}