@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0> .
@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:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_head {
   this: np:hasAssertion dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_assertion ;
    np:hasProvenance dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_provenance ;
    np:hasPublicationInfo dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_assertion a np:Assertion .
  dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_provenance a np:Provenance .
  dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_assertion {
   miriam-gene:2956 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
  dgn-gda:DGN2e842af9e7aff7b95c0bf06061476134 sio:SIO_000628 miriam-gene:2956 , lld:C1527249 ;
    a sio:SIO_001121 .
}
dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_provenance {
   dgn-np:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_assertion dcterms:description "[Hereditary non-polyposis colorectal cancer is the most common known genetic syndrome that predisposes to various types of cancer including gastric cancer and occures mainly due to pathogenic germline mutations in DNA mismatch repair (MMR) genes, such as MLH1, MSH2 and MSH6.]. 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:21136174 ;
    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:NP857391.RAMYv5B0gkZWsVyEXCeRoQFzuGbo5eZsszh6x9Lt579y0130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:13+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" .
}