@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc> .
@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:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_head {
  this: np:hasAssertion dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_assertion;
    np:hasProvenance dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_provenance;
    np:hasPublicationInfo dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_assertion a np:Assertion .
  
  dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_provenance a np:Provenance .
  
  dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_assertion {
  miriam-gene:862 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGNd46ef041da225630b951712a918c0dbd sio:SIO_000628 miriam-gene:862, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_provenance {
  dgn-np:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_assertion dcterms:description
      "[Patient specific oligonucleotide primers were designed based on the complementarity determining regions (CDR) of each MM Ig sequence and used to amplify DNA by polymerase chain reaction for the detection of malignant cells.]. 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:7524734;
    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:NP363735.RAWw8CudBiWEHI4tX7hZvlegkwK--tp8A6lln4w_KYjcc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:33+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" .
}