Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_assertion> ?p ?o ?g. }
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- NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_assertion type Assertion NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_head.
- NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_assertion description "[Mutation analyses for SCA1, 2, 3, 6, 7, 8, 10, 12, 17, and DRPLA and frataxin genes were performed for 251 unrelated Finnish patients who presented with progressive ataxia disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_provenance.
- NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_assertion evidence source_evidence_literature NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_provenance.
- NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_assertion SIO_000772 15691283 NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_provenance.
- NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_assertion wasDerivedFrom befree-2016 NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_provenance.
- NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_assertion wasGeneratedBy ECO_0000203 NP479297.RAUoR8qtiTp78Bs-rq5H1UrnJhU612P5mw7-rtp9Xnbio130_provenance.