@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk> .
@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:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_head {
   this: np:hasAssertion dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_assertion ;
    np:hasProvenance dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_provenance ;
    np:hasPublicationInfo dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_assertion a np:Assertion .
  dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_provenance a np:Provenance .
  dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_assertion {
   miriam-gene:54474 a ncit:C16612 .
  lld:C0027819 a ncit:C7057 .
  dgn-gda:DGNb48b2b90c5db2729d3466072451b954a sio:SIO_000628 miriam-gene:54474 , lld:C0027819 ;
    a sio:SIO_001121 .
}
dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_provenance {
   dgn-np:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_assertion dcterms:description "[Using a panel of mononclonal antibodies, it was also possible to confirm the nature of the infiltration in paraffin sections and to differentiate it from other childhood small round cell tumors, especially neuroblastoma in paraffin sections (typical staining pattern: CD45-, CD43+, vW Factor, Ulex europeus I+, CD20-, CD45RO-, synaptophysin-, chromogranin-, cytokeratin-, desmin-).]. 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:1510033 ;
    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:NP722286.RA9-bhZ8EIXhV8jM5z6PuzR0KHEwURbsB4AFqOFrlPnyk130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:18+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" .
}