@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk> .
@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:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_head {
  this: np:hasAssertion dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_assertion ;
    np:hasProvenance dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_provenance ;
    np:hasPublicationInfo dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_assertion a np:Assertion .
  dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_provenance a np:Provenance .
  dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  lld:C0007102 a ncit:C7057 .
  dgn-gda:DGN95fcb05a672b8194f21f196346046577 sio:SIO_000628 miriam-gene:4360 , lld:C0007102 ;
    a sio:SIO_001121 .
}
dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_provenance {
  dgn-np:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_assertion dcterms:description "[Here, we take a step toward an analogous system for the mismatch repair (MMR) genes (MLH1, MSH2, MSH6, and PMS2) that confer colon cancer susceptibility in Lynch syndrome by calibrating in silico tools to estimate prior probabilities of pathogenicity for MMR gene missense substitutions.]. 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:22949387 ;
    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:NP157518.RACxCf-Qma2QVcTNS4OOpaGnR0L90XNd8ts6YajyaIZOk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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" .
}