@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ> .
@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:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_head {
  this: np:hasAssertion dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_assertion ;
    np:hasProvenance dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_assertion a np:Assertion .
  dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_provenance a np:Provenance .
  dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_assertion {
  miriam-gene:64407 a ncit:C16612 .
  lld:C0041107 a ncit:C7057 .
  dgn-gda:DGNe866b2c33fade8723de5eab23d682c0f sio:SIO_000628 miriam-gene:64407 , lld:C0041107 ;
    a sio:SIO_001121 .
}
dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_provenance {
  dgn-np:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_assertion dcterms:description "[By analyzing several genes with very high (`spiked`) expression in individual cases, we identified clusters with different biologic characteristics, such as samples with MALT1 translocations having high expression of MALT1 and RARA, samples with plasmacytic differentiation having high FKBP11 expression, and samples with high RGS13 expression tending to have trisomy 3 and reactive follicles.]. 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:18974375 ;
    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:NP796370.RAEv-4ZbSe48ZaQaKRyLe4JzXUwWACl5glA7yx4rk1vNQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:09+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" .
}