@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24> .
@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:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_head {
  this: np:hasAssertion dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_assertion;
    np:hasProvenance dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_provenance;
    np:hasPublicationInfo dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_assertion a np:Assertion .
  
  dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_provenance a np:Provenance .
  
  dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_assertion {
  miriam-gene:55655 a ncit:C16612 .
  
  lld:C0024305 a ncit:C7057 .
  
  dgn-gda:DGN1d88ec859ea9f147fc3f78399684624d sio:SIO_000628 miriam-gene:55655, lld:C0024305;
    a sio:SIO_001121 .
}

dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_provenance {
  dgn-np:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_assertion dcterms:description
      "[A panel of six common polymorphisms spanning the NBS1 gene was genotyped and provided no evidence for loss of heterozygosity in the NHL cases with mutations or in the NHL population overall.]. 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:12353271;
    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:NP360582.RAWWYsBmHPEPW8-BQC2ubkcIgifmNYAE8xqv97Z9Gbc24130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:31+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" .
}