@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ> .
@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:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_head {
  this: np:hasAssertion dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_assertion ;
    np:hasProvenance dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_assertion a np:Assertion .
  dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_provenance a np:Provenance .
  dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_assertion {
  miriam-gene:6745 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGNaeac0698c56bcaca3f44671c7539be2e sio:SIO_000628 miriam-gene:6745 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_provenance {
  dgn-np:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_assertion dcterms:description "[From a practical perspective, assessment of the CA SSR I number of CA dinucleotide repeats as a predictor for clinical outcome is very attractive because it is a constant feature that does not change over time and can be easily measured in normal and cancer tissues (blood cells, skin, and tumor biopsies) in an assay that is technically simple, objective, and even quantitative.]. 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:17189396 ;
    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:NP782259.RAgfLJWc_T-4UklO4lFgFOdXt-ksZFk_2ribS08wFopYQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:54+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> ;
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}