@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g> .
@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:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_head {
  this: np:hasAssertion dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_assertion ;
    np:hasProvenance dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_provenance ;
    np:hasPublicationInfo dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_assertion a np:Assertion .
  dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_provenance a np:Provenance .
  dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_assertion {
  miriam-gene:2956 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
  dgn-gda:DGNd0933e53c5968cf6d30e8864c3a657cb sio:SIO_000628 miriam-gene:2956 , lld:C1527249 ;
    a sio:SIO_001121 .
}
dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_provenance {
  dgn-np:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_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:NP442147.RAvZwd6qUDrkvh27h3776M2J4KYBj_1_QnpjmvBG33e7g130_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" .
}