Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.
- NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_assertion description "[The results of screening for mutations in the nuclear genes associated with PEO and multiple mitochondrial DNA deletions, including those in POLG (polymerase gamma gene), ANT1 (gene encoding adenine nucleotide translocator 1), and PEO1, were negative, but sequencing of POLG2 revealed a G1247C mutation in exon 7, resulting in the substitution of a highly conserved glycine with an alanine at codon 416 (G416A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.
- NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_assertion evidence source_evidence_literature NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.
- NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_assertion SIO_000772 18195150 NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.
- NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_assertion wasDerivedFrom befree-2016 NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.
- NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_assertion wasGeneratedBy ECO_0000203 NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.
- befree-2016 importedOn "2016-02-19" NP649944.RActPv67TkxUTaVTSqoJ9uGOpqI3Vdr0qiPn1G1azvObU130_provenance.