@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc> .
@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:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_head {
  this: np:hasAssertion dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_assertion;
    np:hasProvenance dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_provenance;
    np:hasPublicationInfo dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_assertion a np:Assertion .
  
  dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_provenance a np:Provenance .
  
  dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_assertion {
  miriam-gene:49 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
  dgn-gda:DGN97fe64cc30eec0374f569a8353ae7b72 sio:SIO_000628 miriam-gene:49, lld:C0008626;
    a sio:SIO_001121 .
}

dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_provenance {
  dgn-np:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_assertion dcterms: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:NP301930.RA7YpDwLoAl8OlThdiCJkMbt9AmwOoC8wrd3HPn5h-Lrc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:51+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" .
}