@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI> .
@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:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_head {
        this: np:hasAssertion dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_assertion ;
                np:hasProvenance dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_provenance ;
                np:hasPublicationInfo dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_publicationInfo ;
                a np:Nanopublication .

        dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_assertion a np:Assertion .

        dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_provenance a np:Provenance .

        dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_assertion {
        miriam-gene:4885 a ncit:C16612 .

        lld:C1883552 a ncit:C7057 .

        dgn-gda:DGN011a38aec86b971a8d96339204a6b393 sio:SIO_000628 miriam-gene:4885 , lld:C1883552 ;
                a sio:SIO_001121 .
}

dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_provenance {
        dgn-np:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_assertion dcterms:description "[We performed 13 prenatal diagnoses for the NARP (neurogenic weakness, ataxia, retinitis pigmentosa) m.8993T-->G mtDNA mutation (p.Leu156Arg) in the ATP synthase subunit 6 gene.]. 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:17545557 ;
                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:NP940023.RAOc-0FFscmxA46PLX7nZMeDgLauxcJjZSzd2W5Q2IJcI130_publicationInfo {
        this: dcterms:created "2014-10-02T12:41:36+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"^^xsd:string .

        dgn-void:disgenetrdf pav:version "v2.1.0"^^xsd:string .
}
