@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_head {
  this: np:hasAssertion dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_assertion ;
    np:hasProvenance dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_provenance ;
    np:hasPublicationInfo dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_assertion a np:Assertion .
  dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_provenance a np:Provenance .
  dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  lld:C1333990 a ncit:C7057 .
  dgn-gda:DGNa3dc48f2b66c7fed8e771eea31f3b9ea sio:SIO_000628 miriam-gene:4292 , lld:C1333990 ;
    a sio:SIO_001121 .
}
dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_provenance {
  dgn-np:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_assertion dcterms:description "[This clinical case review aimed to identify phenotypic variations in colorectal and extracolonic cancer expression between hereditary nonpolyposis colorectal cancer (HNPCC) families with MLH1 and MSH2 germline mutations and the general population.]. 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:9559626 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1393740.RAc9qyyk0FR1j4Gg_ViFhebuqTJf-UbLZWAMuq6lI9nbs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:18+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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 "v4.0.0.0" .
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}