Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- befree-2016 importedOn "2016-02-19" NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion wasGeneratedBy ECO_0000203 NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion wasDerivedFrom befree-2016 NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion SIO_000772 22405087 NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion evidence source_evidence_literature NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.
- NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_assertion description "[Infantile cerebellar-retinal degeneration associated with a mutation in mitochondrial aconitase, ACO2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966621.RAwSnvXf8aa_2t0JZUN_iGl20i-4bLLHiLYC0vyvWsbUA130_provenance.