@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q> .
@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:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_head {
  this: np:hasAssertion dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_assertion;
    np:hasProvenance dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_provenance;
    np:hasPublicationInfo dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_assertion a np:Assertion .
  
  dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_provenance a np:Provenance .
  
  dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_assertion {
  miriam-gene:4070 a ncit:C16612 .
  
  lld:C0339273 a ncit:C7057 .
  
  dgn-gda:DGNce1dcc9f9f8692302393d3c0b29412bd sio:SIO_000628 miriam-gene:4070, lld:C0339273;
    a sio:SIO_001121 .
}

dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_provenance {
  dgn-np:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_assertion dcterms:description
      "[Although the M1S1 gene was responsible for GDLD in Vietnamese patients, the mutation found here is completely different from that previously reported in Japanese patients, where GDLD is most frequently seen.]. 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:12614764;
    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:NP471196.RAomHG4EJq9LClzb_TatYsNy_OD3ooW0ouHWox1SjnO1Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:42+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" .
}