@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ> .
@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:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_head {
  this: np:hasAssertion dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_assertion;
    np:hasProvenance dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_provenance;
    np:hasPublicationInfo dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_assertion a np:Assertion .
  
  dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_provenance a np:Provenance .
  
  dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGNf57fb27dbf50d92e3831695f63c1912d sio:SIO_000628 miriam-gene:2272, lld:C1961102;
    a sio:SIO_001121 .
}

dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_provenance {
  dgn-np:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_assertion dcterms:description
      "[Although intact FHIT mRNA was detected as the main band in the remaining 37 samples, 33 of them (14 of 14 AML, 11 of 13 chronic myeloid leukemia, five of five acute lymphocytic leukemia, and three of five CLL) expressed aberrant FHIT delta 3-6 mRNA.]. 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:9170214;
    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:NP929522.RAGtpBYtmpZCFmkG00EfZUX0s9VM8l81mfZRK5AOb0ROQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:30+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" .
}