@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_head {
  this: np:hasAssertion dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_assertion ;
    np:hasProvenance dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_provenance ;
    np:hasPublicationInfo dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_assertion a np:Assertion .
  dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_provenance a np:Provenance .
  dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_assertion {
  miriam-gene:6223 a ncit:C16612 .
  lld:C0029463 a ncit:C7057 .
  dgn-gda:DGN8921048dd36d0d5a3866b0c8acb08288 sio:SIO_000628 miriam-gene:6223 , lld:C0029463 ;
    a sio:SIO_001121 .
}
dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_provenance {
  dgn-np:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_assertion dcterms:description "[The role of mutations in RPS19 in erythropoiesis or developmental defects in DBA patients is not obvious, and the increased frequency of osteogenic sarcomas suggests that at least that subset of patients may have a mutant tumor suppressor gene (such as p53, the mutant gene in Li-Fraumeni syndrome) [68].]. 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:12430621 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP374273.RAAHP8JLQBQrXkzor4KrfY8J40MA7LeqtnpvdRaHbQWa4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:35+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}