@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo> .
@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:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_head {
  this: np:hasAssertion dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_assertion ;
    np:hasProvenance dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_provenance ;
    np:hasPublicationInfo dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_assertion a np:Assertion .
  dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_provenance a np:Provenance .
  dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_assertion {
  miriam-gene:54658 a ncit:C16612 .
  lld:C0476089 a ncit:C7057 .
  dgn-gda:DGN545fd20ce163bc7a82b4e5d4dab33713 sio:SIO_000628 miriam-gene:54658 , lld:C0476089 ;
    a sio:SIO_001122 .
}
dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_provenance {
  dgn-np:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_assertion dcterms:description "[These findings define those populations with a high frequency of hemoglobin E-beta-thalassemia and related disorders that are at increased risk for hyperbilirubinemia and gall bladder disease and provide evolutionary insights into how these polymorphisms have arisen and are so unequally distributed among human 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:12850492 ;
    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:NP62265.RAXp9ePIum4aj0kZ2blNXaFk-ayl5RZoGxioQZex6i-jo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}