Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.
- NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_assertion description "[A pronounced lack of Frataxin causes Friedreich's Ataxia, which is a human neurodegenerative and hereditary disease mainly affecting the equilibrium, coordination, muscles and heart.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.
- NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_assertion evidence source_evidence_literature NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.
- NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_assertion SIO_000772 23463383 NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.
- NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_assertion wasDerivedFrom befree-2016 NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.
- NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_assertion wasGeneratedBy ECO_0000203 NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1058066.RA1IBrxaBGG2_LRnd7PDZeHt2uWkFeYnxyuDtTF9NMkVw130_provenance.