@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18> .
@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 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:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_head {
  this: np:hasAssertion dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_assertion;
    np:hasProvenance dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_provenance;
    np:hasPublicationInfo dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_assertion a np:Assertion .
  
  dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_provenance a np:Provenance .
  
  dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_assertion {
  miriam-gene:49 a ncit:C16612 .
  
  lld:C0334108 a ncit:C7057 .
  
  dgn-gda:DGN1a2f00f8713bf56311b9f69265c1ab33 sio:SIO_000628 miriam-gene:49, lld:C0334108;
    a sio:SIO_001121 .
}

dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_provenance {
  dgn-np:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_assertion dct:description
      "[A total of 57 different strains (33 from patients and 24 from healthy members of ACR families not at an increased risk for colon polyposis) were tested for their frequencies of spontaneous structural chromosome aberrations, i.e., chromatid and isochromatid gaps, breaks, and interchanges.]. 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:4016717;
    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:NP358739.RACvzpPaNB4-slG8fjuBVNeUYP9J4CgK9aApGzZZt1i18130_publicationInfo {
  this: dct:created "2014-10-02T12:35:30+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}