@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc> .
@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:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_head {
   this: np:hasAssertion dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_assertion ;
    np:hasProvenance dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_provenance ;
    np:hasPublicationInfo dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_assertion a np:Assertion .
  dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_provenance a np:Provenance .
  dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_assertion {
   miriam-gene:84168 a ncit:C16612 .
  lld:C0025202 a ncit:C7057 .
  dgn-gda:DGNf623ef31af2ab7b2252f0dd2e7f80d22 sio:SIO_000628 miriam-gene:84168 , lld:C0025202 ;
    a sio:SIO_001121 .
}
dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_provenance {
   dgn-np:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_assertion dcterms:description "[We have investigated frameshift mutations in exonic repeats in the ATR, BRCA1, BRCA2, PTCH, CTCF, Cx26, NuMa and TGFbetaRII genes, using human tumor samples from stomach, esophagus, breast and skin and melanoma, as well as colon cancer and endometrial cancer cell lines (125 samples in total).]. 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:10545425 ;
    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:NP395747.RADJ-4fUtiEn22M0DqDJK-E5aHujlzrH9FeKlVWHJRWFc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:55+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" .
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}