@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk> .
@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:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_head {
  this: np:hasAssertion dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_assertion ;
    np:hasProvenance dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_provenance ;
    np:hasPublicationInfo dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_assertion a np:Assertion .
  dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_provenance a np:Provenance .
  dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_assertion {
  miriam-gene:1376 a ncit:C16612 .
  lld:C0026986 a ncit:C7057 .
  dgn-gda:DGN9562c14e7af3ca8e85dbed92ab5a959c sio:SIO_000628 miriam-gene:1376 , lld:C0026986 ;
    a sio:SIO_001121 .
}
dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_provenance {
  dgn-np:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_assertion dcterms:description "[Considering the risk of acquiring a myelodysplastic syndrome (MDS) with age, the aim of this study was to quantify mRNA synthesis of the carnitine palmitoyltransferases (CPT1 and CPT2), carnitine acetyltransferase (CRAT), human specific microsomal CPT, and OCTN2 (organic cation transporter) in mononuclear cells of healthy humans of different age groups and MDS 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:12802501 ;
    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:NP304526.RAbEVYfOjK_R6k7XNuD01uZvJA5gGm3b4yKv_C-58__Wk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:55+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" .
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}