@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis> .
@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:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_head {
  this: np:hasAssertion dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_assertion ;
    np:hasProvenance dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_provenance ;
    np:hasPublicationInfo dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_assertion a np:Assertion .
  dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_provenance a np:Provenance .
  dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_assertion {
  miriam-gene:3265 a ncit:C16612 .
  lld:C0023418 a ncit:C7057 .
  dgn-gda:DGN63dc54d0e295ccd60d00233d1f093bfe sio:SIO_000628 miriam-gene:3265 , lld:C0023418 ;
    a sio:SIO_001121 .
}
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_provenance {
  dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_assertion dcterms:description "[By using a strategy for analysis of gene mutation based on in vitro amplification of target sequences by the polymerase chain reaction (PCR) and selective oligonucleotide hybridization we analyzed the mutational status of codons 12, 13, and 61 of Ha-ras, K-ras, and N-ras in peripheral blood (PB) and/or bone marrow (BM) in 34 cases of primary MDS.]. 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:3285909 ;
    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:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:58+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" .
}