@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs> .
@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:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_head {
  this: np:hasAssertion dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_assertion;
    np:hasProvenance dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_provenance;
    np:hasPublicationInfo dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_assertion a np:Assertion .
  
  dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_provenance a np:Provenance .
  
  dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_assertion {
  miriam-gene:28 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGN29684bd0af9e2332f031c62ad26580a8 sio:SIO_000628 miriam-gene:28, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_provenance {
  dgn-np:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_assertion dcterms:description
      "[Corresponding positions of nonhuman primates have G and C, suggesting that the Se(375) allele is one of the ancestral alleles, reflecting the early human migration from Africa to New Guinea and the long isolation of Dani populations from neighboring populations.]. 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:14569463;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP49722.RAhmd2xXATmbVCLkkd40hMlqmlP_PMlIUDDx3FOeyHtQs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}