@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM> .
@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/v3.0.0/void/> .

dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_head {
  this: np:hasAssertion dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_assertion;
    np:hasProvenance dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_provenance;
    np:hasPublicationInfo dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_assertion a np:Assertion .
  
  dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_provenance a np:Provenance .
  
  dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C0153567 a ncit:C7057 .
  
  dgn-gda:DGNb9d956c4b413f77ba9b43d92e4421e31 sio:SIO_000628 miriam-gene:4292, lld:C0153567;
    a sio:SIO_001122 .
}

dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_provenance {
  dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_assertion dcterms:description
      "[The MLH1 D132H risk variant has significantly lower allele frequency in American compared with Israeli cancer patients and, alone, is unlikely to explain significant amounts of American sporadic colorectal cancer or uterine cancer susceptibility.]. 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:15991064;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:12+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}