@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA> .
@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:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_head {
  this: np:hasAssertion dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_assertion ;
    np:hasProvenance dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_provenance ;
    np:hasPublicationInfo dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_assertion a np:Assertion .
  dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_provenance a np:Provenance .
  dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_assertion {
  miriam-gene:387569 a ncit:C16612 .
  lld:C1333990 a ncit:C7057 .
  dgn-gda:DGN78266468b1430f86e6a6d1be3014915c sio:SIO_000628 miriam-gene:387569 , lld:C1333990 ;
    a sio:SIO_001121 .
}
dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_provenance {
  dgn-np:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_assertion dcterms:description "[The aims of this study are to characterize the frequency, density, and distribution of aberrant crypt foci (ACF) and its histological features and to determine the frequency of loss of expression of DNA mismatch repair (MMR) proteins of subjects with hereditary nonpolyposic colorectal cancer (HNPCC) and sporadic colon rectal cancer (CRC).]. 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:21744313 ;
    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:NP359399.RAGW3zdPFqMVklDqrh5rOYtOX4ZB8eYor7gcTPnMV2HRA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:30+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" .
}