@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE> .
@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:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_head {
  this: np:hasAssertion dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_assertion;
    np:hasProvenance dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_provenance;
    np:hasPublicationInfo dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_assertion a np:Assertion .
  
  dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_provenance a np:Provenance .
  
  dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_assertion {
  miriam-gene:947 a ncit:C16612 .
  
  lld:C0023480 a ncit:C7057 .
  
  dgn-gda:DGNc0dd23daec312901e7d46f868270d65a sio:SIO_000628 miriam-gene:947, lld:C0023480;
    a sio:SIO_001121 .
}

dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_provenance {
  dgn-np:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_assertion dcterms:description
      "[RNA-seq analyses of telomere dysfunctional CMP identified aberrantly spliced transcripts linked to pathways relevant to MDS pathogenesis such as genome stability, DNA repair, chromatin remodeling, and histone modification, which are also enriched in mouse CMP haploinsufficient for SRSF2 and in CD34(+) CMML patient cells harboring SRSF2 mutation.]. 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:25965571;
    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:NP1283593.RAcynYnN2TSuKOYr2SIv1lT6g1ETYWt_B2wB3HLLPUMtE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:28+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" .
}