@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc> .
@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:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_head {
  this: np:hasAssertion dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_assertion;
    np:hasProvenance dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_provenance;
    np:hasPublicationInfo dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_assertion a np:Assertion .
  
  dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_provenance a np:Provenance .
  
  dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_assertion {
  miriam-gene:126 a ncit:C16612 .
  
  lld:C0152018 a ncit:C7057 .
  
  dgn-gda:DGN7116897964c8af4811dfe4107aef9b0f sio:SIO_000628 miriam-gene:126, lld:C0152018;
    a sio:SIO_001121 .
}

dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_provenance {
  dgn-np:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_assertion dcterms:description
      "[Using a population-based case-control study with 858 EC cases and 1,081 controls conducted in Jiangsu Province, China, we aimed to provide further information on the association of ADH1B (rs1229984), ADH1C (rs698) and ALDH2 (rs671) polymorphisms with EC in a Chinese population.]. 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:22930414;
    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:NP649788.RAtt6P_X7dFd99BMpNe6zrTRP6T0wMxa6EyHLn-TDTSHc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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" .
}