@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E> .
@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:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_head {
  this: np:hasAssertion dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_assertion;
    np:hasProvenance dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_provenance;
    np:hasPublicationInfo dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_assertion a np:Assertion .
  
  dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_provenance a np:Provenance .
  
  dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0265325 a ncit:C7057 .
  
  dgn-gda:DGN24fdd14ea777acdd7f171897d7412287 sio:SIO_000628 miriam-gene:4360, lld:C0265325;
    a sio:SIO_001121 .
}

dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_provenance {
  dgn-np:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_assertion dcterms:description
      "[The former appears to be mostly due to mutations in the APC gene, and the latter to mutations in mismatch repair (MMR) genes, so it would be better named as hereditary mismatch repair deficiency (HMRDS).]. 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:15648180;
    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:NP352691.RARzEQStVg0BqH3ucCv7jo8eBqH75z8aODaZprDzJbJ3E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:27+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" .
}