http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#head
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#assertion
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#provenance
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#assertion
http://rdf.disgenet.org/resource/gda/DGNc7f8d70bd7a278bd7a11d3f155ec0227
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/5428
http://rdf.disgenet.org/resource/gda/DGNc7f8d70bd7a278bd7a11d3f155ec0227
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0030567
http://rdf.disgenet.org/resource/gda/DGNc7f8d70bd7a278bd7a11d3f155ec0227
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001121
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#provenance
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#assertion
http://purl.org/dc/terms/description
[Recently identified nuclear gene mutations of mitochondrial proteins include mutations of frataxin causing Friedreich's ataxia, PINK1, DJ1 causing Parkinson's disease and POLG causing infantile mtDNA depletion syndrome, ophthalmoplegia, parkinsonism, male subfertility and, in a transgenic mouse model, premature senescence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#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/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/16815381
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#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/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/dc/terms/created
2017-10-17T13:15:31+02:00
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP836708.RAd8szlOIEx7p2D6NdwPpGwlVSHCvUkqUe9B4vWowrL54
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