Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.
- NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_assertion description "[This review focuses on our current understanding of nuclear gene mutations that produce mtDNA alterations and cause mitochondrial depletion syndrome (MDS), progressive external ophthalmoplegia (PEO), ataxia-neuropathy, or mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.
- NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_assertion evidence source_evidence_literature NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.
- NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_assertion SIO_000772 17892433 NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.
- NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_assertion wasDerivedFrom befree-20140225 NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.
- NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_assertion wasGeneratedBy ECO_0000203 NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP746034.RALdJhQMypr2f5K5TgGHZxx36XcFytBYrKtAwD-2w-d8k130_provenance.