Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_assertion> ?p ?o ?g. }
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- NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_assertion type Assertion NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_head.
- NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_assertion description "[This is the first description of a family with two SCA mutations with affected subjects having a combined SCA2 and SCA10 phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_provenance.
- NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_assertion evidence source_evidence_literature NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_provenance.
- NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_assertion SIO_000772 25630585 NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_provenance.
- NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_assertion wasDerivedFrom befree-2016 NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_provenance.
- NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_assertion wasGeneratedBy ECO_0000203 NP1259139.RA8bYvwk3hcQOlrJlwv13yhB42JZBj9bpF8E5YcmKauAo130_provenance.