@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4> .
@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:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_head {
  this: np:hasAssertion dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_assertion;
    np:hasProvenance dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_provenance;
    np:hasPublicationInfo dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_assertion a np:Assertion .
  
  dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_provenance a np:Provenance .
  
  dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_assertion {
  miriam-gene:861 a ncit:C16612 .
  
  lld:C0026985 a ncit:C7057 .
  
  dgn-gda:DGNc3f0e53f4a8c00e71e4409e570cdd74d sio:SIO_000628 miriam-gene:861, lld:C0026985;
    a sio:SIO_001121 .
}

dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_provenance {
  dgn-np:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_assertion dcterms:description
      "[Furthermore, an increased awareness of clinicians has helped detect a number of additional families affected by inherited myelodysplastic syndromes, resulting in the identification of novel causative mechanisms of disease, such as RUNX1 deficiency resulting from constitutional microdeletions of 21q22 and myelodysplasia-associated with telomerase deficiency.]. 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:21606161;
    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:NP896267.RAjrb3JDJUpH9ydlce4JZrr3eAeYeuiUaFoS7qdFhubH4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:30+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: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" .
}