http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#head
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#assertion
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#provenance
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#assertion
http://rdf.disgenet.org/resource/gda/DGNe3cb4cc747904d5b5745bbc583317bc1
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/80207
http://rdf.disgenet.org/resource/gda/DGNe3cb4cc747904d5b5745bbc583317bc1
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0338508
http://rdf.disgenet.org/resource/gda/DGNe3cb4cc747904d5b5745bbc583317bc1
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#provenance
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#assertion
http://purl.org/dc/terms/description
[We found a common coupling defect of oxidative phosphorylation in fibroblasts of patients affected by autosomal dominant optic atrophy (mutations of OPA1), autosomal dominant optic atrophy associated with cataract (mutations of OPA3), and Leber's hereditary optic neuropathy, a disorder associated with point mutations of mitochondrial DNA complex I genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18496845
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/dc/terms/created
2017-10-17T13:18:55+02:00
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1374655.RAe-3F_CKrYZKcvAUl0L3C6FHOgjzaYklvXuent3mRyF4
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0