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- NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_assertion type Assertion NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_head.
- NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_assertion wasGeneratedBy ECO_0000203 NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_provenance.
- NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_assertion wasDerivedFrom befree-2016 NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_provenance.
- NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_assertion SIO_000772 9600245 NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_provenance.
- NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_assertion evidence source_evidence_literature NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_provenance.
- NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_assertion description "[Three novel KCNA1 mutations in episodic ataxia type I families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395849.RABOoXe-LNXhyPeg1HoN10K10LNQOPScsIb_osHkmKiNk130_provenance.