@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc> .
@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:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_head {
  this: np:hasAssertion dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_assertion ;
    np:hasProvenance dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_provenance ;
    np:hasPublicationInfo dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_assertion a np:Assertion .
  dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_provenance a np:Provenance .
  dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_assertion {
  miriam-gene:570 a ncit:C16612 .
  lld:C0476089 a ncit:C7057 .
  dgn-gda:DGNbd9626b31aea71ba9a27dc216b9953a0 sio:SIO_000628 miriam-gene:570 , lld:C0476089 ;
    a sio:SIO_001121 .
}
dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_provenance {
  dgn-np:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_assertion dcterms:description "[In the present study, we analyzed the type (insertions/deletions), size, and frequency of mutations occurring at three BAT and three dinucleotide markers in CRC and EC, to elucidate whether it is possible to establish different MSI profiles in carcinomas of different tissue origin.]. 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:19373783 ;
    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:NP241038.RAHlZiV2-e961z3FK-1qbYRyLUrWFQKrlAETS-xiUkpUc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:15+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" .
}