@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso> .
@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 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:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_head {
  this: np:hasAssertion dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_assertion;
    np:hasProvenance dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_provenance;
    np:hasPublicationInfo dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_assertion a np:Assertion .
  
  dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_provenance a np:Provenance .
  
  dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_assertion {
  miriam-gene:4549 a ncit:C16612 .
  
  lld:C0011053 a ncit:C7057 .
  
  dgn-gda:DGNda9346cf6a07ca455dc3b711e1cc4642 sio:SIO_000628 miriam-gene:4549, lld:C0011053;
    a sio:SIO_001121 .
}

dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_provenance {
  dgn-np:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_assertion dct:description
      "[Samples from 30 deaf probands exhibiting features suggestive of syndromic mitochondrial deafness or from families with maternal transmission of deafness were selected for investigation of mutations in the mitochondrial genes MT-RNR1 and MT-TS1.]. 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:20722495;
    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:NP361091.RABMz9_y7pHrZKT4_0aH1_6N1RyY_DAzGW1BHtu8YiAso130_publicationInfo {
  this: dct:created "2014-10-02T12:35:31+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}