@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs> .
@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:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_head {
  this: np:hasAssertion dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_assertion;
    np:hasProvenance dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_provenance;
    np:hasPublicationInfo dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_assertion a np:Assertion .
  
  dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_provenance a np:Provenance .
  
  dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_assertion {
  miriam-gene:25 a ncit:C16612 .
  
  lld:C0751606 a ncit:C7057 .
  
  dgn-gda:DGN558529c9292167e727d4bfebf3e99328 sio:SIO_000628 miriam-gene:25, lld:C0751606;
    a sio:SIO_001121 .
}

dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_provenance {
  dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_assertion dcterms:description
      "[The diagnosis of the BCR-ABL fusion gene in ALL has important clinical implications because it is the most common molecular genetic change in adult ALL and is associated with short remissions and poor outcome in all age groups.]. 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:1516023;
    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:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:07+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" .
}