@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU> .
@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:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_head {
  this: np:hasAssertion dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion;
    np:hasProvenance dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance;
    np:hasPublicationInfo dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion a np:Assertion .
  
  dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance a np:Provenance .
  
  dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN173c35125f5129f2f1985fb52691f531 sio:SIO_000628 miriam-gene:4292, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_provenance {
  dgn-np:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_assertion dcterms:description
      "[Based on the InSiGHT database and the original references that reported the mutations, we analyzed the distributions of MLH1 and MSH2 mutations in yellow race and white race respectively and compared them subsequently.]. 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:21155023;
    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:NP602828.RAlhV935yc4F2bAsAse_8m3YJ_H1-iVn-Yiw5Ur0CnaXU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:02+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" .
}