@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg> .
@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:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_head {
  this: np:hasAssertion dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_assertion ;
    np:hasProvenance dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_provenance ;
    np:hasPublicationInfo dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_assertion a np:Assertion .
  dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_provenance a np:Provenance .
  dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  lld:C1333990 a ncit:C7057 .
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}
dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_provenance {
  dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_assertion dcterms:description "[There are two major hereditary colorectal cancer syndromes: Adenomatous Polyposis, secondary to APC germline alterations (FAP, Familial Adenomatous Polyposis) or secondary to MUTYH germline alterations (MAP, MUTYH associated Polyposis), and Lynch syndrome, associated with germline mutations in mismatch repair genes (MLH1, MSH2, MSH6 and PMS2).]. 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:19931546 ;
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP777190.RA9xCVN_PS3OnOTLpV3yCejh5GKWm29hSxlmDcrdeoOkg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:37+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}