@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM> .
@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:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_head {
  this: np:hasAssertion dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_assertion;
    np:hasProvenance dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_provenance;
    np:hasPublicationInfo dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_assertion a np:Assertion .
  
  dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_provenance a np:Provenance .
  
  dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN283ca917c86d14d34f1abdb9d1ded34f sio:SIO_000628 miriam-gene:4360, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_provenance {
  dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_assertion dcterms:description
      "[The eponymous Muir-Torre syndrome (MTS) is a clinical variant of hereditary non polyposis colorectal cancer, and is defined as an autosomal dominant condition with simultaneous sebaceous neoplasms of the skin and visceral malignant disease resulting from germline mutations in the DNA mismatch repair (MMR) genes.]. 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:19449129;
    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:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:41+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" .
}