@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_head {
  this: np:hasAssertion dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_assertion;
    np:hasProvenance dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_provenance;
    np:hasPublicationInfo dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_assertion a np:Assertion .
  
  dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_provenance a np:Provenance .
  
  dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_assertion {
  miriam-gene:445347 a ncit:C16612 .
  
  lld:C0242596 a ncit:C7057 .
  
  dgn-gda:DGNbab4e28ea90312d4492407480fe211f8 sio:SIO_000628 miriam-gene:445347, lld:C0242596;
    a sio:SIO_001121 .
}

dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_provenance {
  dgn-np:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_assertion dcterms:description
      "[These data indicate that the assignment of clonal specific markers based upon the sequence of TCRG rearrangements at presentation may not always be useful in the detection of minimal residual disease in ALL.]. 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:8289500;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP644490.RAkt5bGn7xfatGAfcrZ26C6qa6hoaM1JNnfrKD9YGn-a8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:28+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}