@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_head {
  this: np:hasAssertion dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_assertion;
    np:hasProvenance dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_provenance;
    np:hasPublicationInfo dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_assertion a np:Assertion .
  
  dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_provenance a np:Provenance .
  
  dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGNb25c1eef4cef2eb3ee2ebe582d0118ed sio:SIO_000628 miriam-gene:4436, lld:C0024299;
    a sio:SIO_001121 .
}

dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_provenance {
  dgn-np:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_assertion dcterms:description
      "[Twenty-two individuals with non-Hodgkin lymphomas (NHL) and 50 normal individuals were screened for polymorphic variants in exon 13 of the hMSH2 mismatch repair gene in order to determine if there is any association with development of lymphomas.]. 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:11890986;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP569852.RAkKq-njy0PUrRFm8pRofAkxEO9ceF9P6adWHC-2jOp5M130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:19+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}