@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk> .
@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:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_head {
  this: np:hasAssertion dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_assertion;
    np:hasProvenance dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_provenance;
    np:hasPublicationInfo dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_assertion a np:Assertion .
  
  dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_provenance a np:Provenance .
  
  dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_assertion {
  miriam-gene:613 a ncit:C16612 .
  
  lld:C0023473 a ncit:C7057 .
  
  dgn-gda:DGNf14b6d69ef454727896c476831f2795e sio:SIO_000628 miriam-gene:613, lld:C0023473;
    a sio:SIO_001121 .
}

dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_provenance {
  dgn-np:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_assertion dcterms:description
      "[Our data now provide a molecular diagnostic marker for CML-N, and they are consistent with the notion that the inclusion or exclusion of BCR exons in the fusion protein affects dramatically its capacity to derange myeloid proliferation and differentiation, leading to the appearance of different disease phenotypes.]. 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:8839830;
    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:NP1359035.RAMVOyvwTABDlpvllBA_n3YDyBlxuNFewdYGSkCDfrbGk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:02+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" .
}