@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY> .
@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:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_head {
  this: np:hasAssertion dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_assertion;
    np:hasProvenance dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_provenance;
    np:hasPublicationInfo dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_assertion a np:Assertion .
  
  dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_provenance a np:Provenance .
  
  dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_assertion {
  miriam-gene:861 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGNb3c6d5cf2d2b9eeadf61724b77b3a0e6 sio:SIO_000628 miriam-gene:861, lld:C1961102;
    a sio:SIO_001121 .
}

dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_provenance {
  dgn-np:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_assertion dcterms:description
      "[We reasoned that shared clonal rearrangements of IG or TCR genes by concordant ALL in twins would be informative about the fetal cell type in which clonal advantage is elicited by ETV6-RUNX1.]. 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:25388957;
    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:NP1236788.RAwMqpdMKXAcAONpMrtfWUl92ymW3V6My-g4BkcTJ8prY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:06+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" .
}