Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_assertion> ?p ?o ?g. }
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- NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_assertion type Assertion NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_head.
- NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_assertion description "[Based on a nested-PCR approach and direct sequencing, a disease causing mutation at the SCA31 locus could be excluded for the German SCA4 kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_provenance.
- NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_assertion evidence source_evidence_literature NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_provenance.
- NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_assertion SIO_000772 21267591 NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_provenance.
- NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_assertion wasDerivedFrom befree-2016 NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_provenance.
- NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_assertion wasGeneratedBy ECO_0000203 NP867792.RADvFmi6bMdbBrz4UAHK-WL1hxqKsIvoCBK1rDUJKuW6s130_provenance.