Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.
- NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_assertion wasGeneratedBy ECO_0000203 NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.
- NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_assertion wasDerivedFrom befree-20150227 NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.
- NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_assertion SIO_000772 11448300 NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.
- NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_assertion evidence source_evidence_literature NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.
- NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_assertion description "[Machado-Joseph disease-SCA3 was the most common type of autosomal dominant SCA in the Taiwanese cohort, accounting for 35 cases (47.3%), followed by SCA6 (8 [10.8%]), SCA2 (8 [10.8%]), SCA1 (4 [5.4%]), SCA7 (2 [2.7%]), dentatorubropallidoluysian atrophy (1 [1.4%]), and SCA8 (0%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923896.RAdQRQKwTirI9Hh67q9rvatJuB-C_3Gm0UvV1_U52n7-U130_provenance.