Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_assertion> ?p ?o ?g. }
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- NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_assertion type Assertion NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_head.
- NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_assertion description "[Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_provenance.
- NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_assertion evidence source_evidence_curated NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_provenance.
- NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_assertion SIO_000772 9989622 NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_provenance.
- NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_assertion wasDerivedFrom uniprot-20130724 NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_provenance.
- NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_assertion wasGeneratedBy ECO_0000218 NP2434.RAvPn9QHLfedQz5LbU21FzpBgEyjJH1hVbdndGhAnHQhE130_provenance.