@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM> .
@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:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_head {
  this: np:hasAssertion dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_assertion ;
    np:hasProvenance dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_provenance ;
    np:hasPublicationInfo dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_assertion a np:Assertion .
  dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_provenance a np:Provenance .
  dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_assertion {
  miriam-gene:57498 a ncit:C16612 .
  lld:C0023484 a ncit:C7057 .
  dgn-gda:DGN9c01872137330bfb326e9b1aa4375079 sio:SIO_000628 miriam-gene:57498 , lld:C0023484 ;
    a sio:SIO_001121 .
}
dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_provenance {
  dgn-np:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_assertion dcterms:description "[Using allele-specific amplification method (ARMS), a highly sensitive one-stage allele-specific PCR, we have evaluated the incidence of NRAS and KRAS2 activating mutations (codons 12, 13, and 61) in 62 patients with either monoclonal gammopathy of undetermined significance (MGUS) or multiple myeloma (MM), primary plasma-cell leukemia (P-PCL), and also in human myeloma cell lines (HMCL).]. 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:11524732 ;
    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:NP162504.RAJPL42ITlwtwvyUUyCb5mRhceL7gzWQslu0gQEia_mhM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:28+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" .
}