@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY> .
@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:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_head {
  this: np:hasAssertion dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_assertion ;
    np:hasProvenance dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_provenance ;
    np:hasPublicationInfo dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_assertion a np:Assertion .
  dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_provenance a np:Provenance .
  dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_assertion {
  miriam-gene:2956 a ncit:C16612 .
  lld:C1883486 a ncit:C7057 .
  dgn-gda:DGNc7bda45c6448991d76daf8447f112ad3 sio:SIO_000628 miriam-gene:2956 , lld:C1883486 ;
    a sio:SIO_001121 .
}
dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_provenance {
  dgn-np:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_assertion dcterms:description "[Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder predisposing to predominantly colorectal cancer (CRC) and endometrial cancer frequently due to germline mutations in DNA mismatch repair (MMR) genes, mainly MLH1, MSH2 and also MSH6 in families seen to demonstrate an excess of endometrial cancer.]. 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:15118395 ;
    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:NP442153.RAl5aG1HLuJDM13qAvX4IFZSIRzZ5afeFEPPoRU7vlMwY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:05+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:disgenetv3.0rdf ;
    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" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}