@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578> .
@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:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_head {
  this: np:hasAssertion dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_assertion ;
    np:hasProvenance dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_provenance ;
    np:hasPublicationInfo dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_assertion a np:Assertion .
  dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_provenance a np:Provenance .
  dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_assertion {
  miriam-gene:4535 a ncit:C16612 .
  lld:C0581883 a ncit:C7057 .
  dgn-gda:DGN38734460b2ec894c3986dee0b05dab06 sio:SIO_000628 miriam-gene:4535 , lld:C0581883 ;
    a sio:SIO_001121 .
}
dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_provenance {
  dgn-np:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_assertion dcterms:description "[We report here the biochemical characterization of the deafness-associated mitochondrial tRNA(Ser(UCN)) T7511C mutation, in conjunction with homoplasmic ND1 T3308C and tRNA(Ala) T5655C mutations using cybrids constructed by transferring mitochondria from lymphoblastoid cell lines derived from an African family into human mtDNA-less (rho degrees ) cells.]. 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:14960712 ;
    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:NP315907.RAp1x-Qvvl7Y4X9jJhM9A5twE6OZxISyF1Uqw3uXdP578130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
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}