@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4> .
@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:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_head {
  this: np:hasAssertion dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_assertion ;
    np:hasProvenance dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_provenance ;
    np:hasPublicationInfo dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_assertion a np:Assertion .
  dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_provenance a np:Provenance .
  dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGNa8eb8c95c7bbcdf8e60243a6cbfbfe55 sio:SIO_000628 miriam-gene:4436 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_provenance {
  dgn-np:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_assertion dcterms:description "[Screening for germline MLH1, MSH2, MSH6, and PMS2 mutations was performed for all incident CRC cases recruited from cancer registries (population based probands) displaying microsatellite instability (MSI) or loss of expression of MMR genes by immunohistochemistry (IHC) and probands with CRC in multi-case families recruited from clinics (clinic based probands), regardless of MSI or IHC status.]. 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:21636617 ;
    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:NP205206.RAtsx0a9ziawVZt0UftMoifmCvf3LWDngulkp0XpY1AT4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+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" .
}