@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA> .
@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:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_head {
  this: np:hasAssertion dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_assertion ;
    np:hasProvenance dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_provenance ;
    np:hasPublicationInfo dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_provenance a np:Provenance .
  dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_assertion {
  miriam-gene:6936 a ncit:C16612 .
  lld:C0392784 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_provenance {
  dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_assertion dcterms:description "[In conclusion, this study emphasizes 1) the occurrence of adult-type DFSP in children, 2) the close relationship between DFSP and GCF clinically, histologically, and molecularly, 3) the excellent prognostic of these lesions if widely excised, and 4) the diagnostic usefulness of RT-PCR analyses in detecting the gene fusion transcripts resulting from the t(17;22) (q22;q13) in paraffin-embedded tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP589978.RAJ7lM6jyH5MipWd1GCqHqH3ubxxXJWdD9dC91FzZNeBA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:55+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> ;
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}