@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c> .
@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:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_head {
  this: np:hasAssertion dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_assertion ;
    np:hasProvenance dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_provenance ;
    np:hasPublicationInfo dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_assertion a np:Assertion .
  dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_provenance a np:Provenance .
  dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_assertion {
  miriam-gene:2120 a ncit:C16612 .
  lld:C0023449 a ncit:C7057 .
  dgn-gda:DGNf4f1650fc34a9f0b0721003e8df4e614 sio:SIO_000628 miriam-gene:2120 , lld:C0023449 ;
    a sio:SIO_001121 .
}
dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_provenance {
  dgn-np:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_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:NP1236790.RArGEh6a8Y71PlhoHlVLd_lpVDoNGu_pcLHhdxNMvgY_c130_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" .
}