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- NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_assertion type Assertion NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_head.
- NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_assertion wasGeneratedBy ECO_0000203 NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_provenance.
- NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_assertion wasDerivedFrom befree-20150227 NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_provenance.
- NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_assertion SIO_000772 21717286 NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_provenance.
- NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_assertion evidence source_evidence_literature NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_provenance.
- NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_assertion description "[A total of 184 individuals were eligible for presymptomatic testing due to a risk for spinocerebellar ataxia (SCA) - SCA3 (80%), Huntington's disease (11.9%), familial amyloidotic neuropathy (4.3%), SCA1, SCA2, SCA6, or SCA7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557336.RA6NHMJLo4_Aexw82mUyW1m-aPiFoZTnYYVHAfrvuoLFE130_provenance.