@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0> .
@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:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_head {
  this: np:hasAssertion dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion;
    np:hasProvenance dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_provenance;
    np:hasPublicationInfo dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion a np:Assertion .
  
  dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_provenance a np:Provenance .
  
  dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion {
  miriam-gene:4851 a ncit:C16612 .
  
  lld:C0023434 a ncit:C7057 .
  
  dgn-gda:DGN057cabea2fb82fa97101ebe494d5a856 sio:SIO_000628 miriam-gene:4851, lld:C0023434;
    a sio:SIO_001121 .
}

dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_provenance {
  dgn-np:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_assertion dcterms:description
      "[These findings indicate that the distribution of NOTCH1 mutations in CLL with trisomy 12 is heterogeneous and that the presence of additional chromosomal abnormalities such as trisomy 18 could change the prognosis of these patients.]. 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:22619094;
    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:NP266393.RAO8007cMpxYyRVRytjZtIt34vLMchw2GXAa_czUbNHF0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}