@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE> .
@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:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_head {
  this: np:hasAssertion dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_assertion;
    np:hasProvenance dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_provenance;
    np:hasPublicationInfo dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_assertion a np:Assertion .
  
  dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_provenance a np:Provenance .
  
  dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_assertion {
  miriam-gene:54658 a ncit:C16612 .
  
  lld:C0022353 a ncit:C7057 .
  
  dgn-gda:DGN75f546388401003e1b3d272e01d53e37 sio:SIO_000628 miriam-gene:54658, lld:C0022353;
    a sio:SIO_001122 .
}

dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_provenance {
  dgn-np:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_assertion dcterms:description
      "[Mutation of the UGT1A1 gene, glycine to arginine at codon 71 (G71R), is related to the development of neonatal jaundice in East Asian populations but the frequency of this mutation is rare among Caucasian 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:20528217;
    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:NP912872.RAS0kwhTNvz3cCnBjBY0ThGF1WQHEnp6qXuuOZ8b5ATWE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:57+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" .
}