@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo> .
@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:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_head {
  this: np:hasAssertion dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_assertion ;
    np:hasProvenance dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_provenance ;
    np:hasPublicationInfo dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_assertion a np:Assertion .
  dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_provenance a np:Provenance .
  dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_assertion {
  miriam-gene:5925 a ncit:C16612 .
  lld:C0027831 a ncit:C7057 .
  dgn-gda:DGNe33dc9734a21373ec8e73bc44cdee53b sio:SIO_000628 miriam-gene:5925 , lld:C0027831 ;
    a sio:SIO_001121 .
}
dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_provenance {
  dgn-np:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_assertion dcterms:description "[We have analyzed the somatic mutations in 89 cutaneous neurofibromas derived from three unrelated NF1 patients with high tumor burden, by loss of heterozygosity (LOH) analysis of the NF1, TP53, RB1, and CDKN2A genes, by assessing microsatellite instability (MSI), by direct sequencing of the NF1, TP53, and several mismatch repair (MMR) genes and by multiplex ligation-dependent probe amplification of the NF1 and TP53 genes.]. 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:20358387 ;
    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:NP237111.RArusIx3hAsGqS85dF8vHLI4k0erjapjO7OpQ2SNzYXuo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}