@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA> .
@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:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_head {
  this: np:hasAssertion dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_assertion ;
    np:hasProvenance dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_provenance ;
    np:hasPublicationInfo dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_assertion a np:Assertion .
  dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_provenance a np:Provenance .
  dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_assertion {
  miriam-gene:9033 a ncit:C16612 .
  lld:C1136084 a ncit:C7057 .
  dgn-gda:DGN8188829508461ddd01af377e204c4488 sio:SIO_000628 miriam-gene:9033 , lld:C1136084 ;
    a sio:SIO_001121 .
}
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_provenance {
  dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_assertion dcterms:description "[To provide insights into the molecular characterization of plasma cell dyscrasias and to investigate the contribution of specific genetic lesions to the biological and clinical heterogeneity of MM, we analysed the gene expression profiles of plasma cells isolated from seven MGUS, 39 MM and six PCL patients by means of DNA microarrays.]. 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:15735737 ;
    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:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:20+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" .
}