@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k> .
@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:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_head {
  this: np:hasAssertion dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_assertion;
    np:hasProvenance dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_provenance;
    np:hasPublicationInfo dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_assertion a np:Assertion .
  
  dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_provenance a np:Provenance .
  
  dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_assertion {
  miriam-gene:6965 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGNc53f41dfa20bc5516fb8df52e16091d7 sio:SIO_000628 miriam-gene:6965, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_provenance {
  dgn-np:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_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:NP300108.RABDqiTawgjrLX-vi61_RhTsxxZDraksT_ezvLA_FD13k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:50+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" .
}