@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4> .
@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:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_head {
  this: np:hasAssertion dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_assertion ;
    np:hasProvenance dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_provenance ;
    np:hasPublicationInfo dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_assertion a np:Assertion .
  dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_provenance a np:Provenance .
  dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_assertion {
  miriam-gene:3492 a ncit:C16612 .
  lld:C0026764 a ncit:C7057 .
  dgn-gda:DGNc925caecc821842e3c2e4d009adb3d9e sio:SIO_000628 miriam-gene:3492 , lld:C0026764 ;
    a sio:SIO_001121 .
}
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_provenance {
  dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_assertion dcterms:description "[To assess the frequency of the t(4;14)(p16.3;q32) translocation in MM, we performed a double-color fluorescent in situ hybridization (FISH) analysis of interphase nuclei with differently labeled probes specific for the IGH locus (a pool of plasmid clones specific for the IGH constant regions) or 4p16.3 (yeast artificial chromosome (YAC) 764-H1 spanning the region involved in breakpoints).]. 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:10397739 ;
    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:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:11+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" .
}