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- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion type Assertion NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_head.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion wasGeneratedBy ECO_0000203 NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion wasDerivedFrom befree-20150227 NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion SIO_000772 10399872 NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion evidence source_evidence_literature NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.