@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_head {
  this: np:hasAssertion dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_assertion;
    np:hasProvenance dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_provenance;
    np:hasPublicationInfo dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_assertion a np:Assertion .
  
  dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_provenance a np:Provenance .
  
  dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_assertion {
  miriam-gene:2120 a ncit:C16612 .
  
  lld:C0014457 a ncit:C7057 .
  
  dgn-gda:DGNcf60d573317a32e6ffa207297203f593 sio:SIO_000628 miriam-gene:2120, lld:C0014457;
    a sio:SIO_001121 .
}

dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_provenance {
  dgn-np:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_assertion dcterms:description
      "[Clinicohematological data in these studies as well as the restriction mapping of chromosomal breakpoints strongly suggest that (1) common features in MDSs involving the TEL gene are monocytosis and eosinophilia, (2) chromosomes other than no.]. 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:7742547;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1320360.RAbRg5shBHpHtcZHfEdZJZNXKopq8QbhN-vGP8dEOvOaU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:45+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}