@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds> .
@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:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_head {
  this: np:hasAssertion dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_assertion ;
    np:hasProvenance dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_provenance ;
    np:hasPublicationInfo dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_assertion a np:Assertion .
  dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_provenance a np:Provenance .
  dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_assertion {
  miriam-gene:55972 a ncit:C16612 .
  lld:C0221018 a ncit:C7057 .
  dgn-gda:DGN7d3f71e0577a9fcf7f3cb00c51a4f838 sio:SIO_000628 miriam-gene:55972 , lld:C0221018 ;
    a sio:SIO_001121 .
}
dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_provenance {
  dgn-np:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_assertion dcterms:description "[Here, by positional cloning, we define a previously unknown form of autosomal recessive nonsyndromic congenital sideroblastic anemia, associated with mutations in the gene encoding the erythroid specific mitochondrial carrier family protein SLC25A38, and demonstrate that SLC25A38 is important for the biosynthesis of heme in eukaryotes.]. 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:19412178 ;
    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:NP224853.RADtdO0mwDpUfGOpOhncEScS5gJU1daqT3N3JJJUc7Uds130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
}