@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U> .
@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:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_head {
  this: np:hasAssertion dgn-np:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_assertion ;
    np:hasProvenance dgn-np:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_provenance ;
    np:hasPublicationInfo dgn-np:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_assertion {
  miriam-gene:6023 a ncit:C16612 .
  lld:C0265290 a ncit:C7057 .
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dgn-np:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_provenance {
  dgn-np:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_assertion dcterms:description "[We examined 12 Japanese patients with metaphyseal chondrodysplasia (MCD) for mutations in the ribonuclease mitochondrial RNA processing gene (RMRP), and identified four novel mutations in two patients with typical and atypical cartilage-hair hypoplasia (CHH), a form of MCD characterized by extra-skeletal manifestations including hypoplastic hair and defective immunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP347836.RADsFwzRYzy41zLU24OHCpyjdFiEI9zJnymOnjTHZLM0U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:24+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}