@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0> .
@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:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_head {
  this: np:hasAssertion dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_assertion ;
    np:hasProvenance dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_provenance ;
    np:hasPublicationInfo dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_assertion a np:Assertion .
  dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_provenance a np:Provenance .
  dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_assertion {
  miriam-gene:3480 a ncit:C16612 .
  lld:C0206656 a ncit:C7057 .
  dgn-gda:DGNef906851a43bb8f6ca015dfe9e2bd335 sio:SIO_000628 miriam-gene:3480 , lld:C0206656 ;
    a sio:SIO_001121 .
}
dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_provenance {
  dgn-np:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_assertion dcterms:description "[In summary, these results indicate that genomic gains and losses involve alike chromosomes with similar frequencies within the histopathologic and genetic subtypes of rhabdomyosarcoma, that genomic amplification is frequent not only in the alveolar histologic subtype of rhabdomyosarcoma but also in ERMS with anaplasia, and that amplification of IGF1R possibly plays a role in the development or progression of a subset of rhabdomyosarcomas.]. 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:11807989 ;
    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:NP599247.RA1-nReas0qVMHVtRjzWKyeD0q3vGUeT_AVNRyv7Dgrt0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:00+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" .
}