@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms> .
@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:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_head {
  this: np:hasAssertion dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_assertion;
    np:hasProvenance dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_provenance;
    np:hasPublicationInfo dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_assertion a np:Assertion .
  
  dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_provenance a np:Provenance .
  
  dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_assertion {
  miriam-gene:211 a ncit:C16612 .
  
  lld:C0002896 a ncit:C7057 .
  
  dgn-gda:DGN1c4bc33354cde240fd7e5b83462d9709 sio:SIO_000628 miriam-gene:211, lld:C0002896;
    a sio:SIO_001121 .
}

dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_provenance {
  dgn-np:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_assertion dcterms:description
      "[X-linked sideroblastic anemias (XLSAs), a group of severe disorders in humans characterized by inadequate formation of heme in erythroblast mitochondria, are caused by mutations in the gene for erythroid eALAS, one of two human genes for ALAS.]. 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:16121195;
    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:NP226950.RAcLoHKoM76MX33enuBRp5hOycGcoVWntuBJ5jAJJpyms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:06+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" .
}