@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o> .
@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:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_head {
  this: np:hasAssertion dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_assertion;
    np:hasProvenance dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_provenance;
    np:hasPublicationInfo dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_assertion a np:Assertion .
  
  dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_provenance a np:Provenance .
  
  dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C0302592 a ncit:C7057 .
  
  dgn-gda:DGNd04a9d8f0916de3aaf5817ffe2056a8d sio:SIO_000628 miriam-gene:2272, lld:C0302592;
    a sio:SIO_001121 .
}

dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_provenance {
  dgn-np:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_assertion dcterms:description
      "[To our knowledge, this is the first report of HDs encompassing the FHIT gene region in primary tumor samples and underscores the usefulness of high resolution genetic analysis of tumor genomes in determining the chromosomal aberrations underlying the malignant progression of CC.]. 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:9307297;
    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:NP237226.RAbNgFOcL7kTvvUi6nMP9rwFg-ZAH2hi1akth-zcOcv1o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}