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- NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_assertion type Assertion NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_head.
- NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_assertion description "[This indel mutation in FHL1 broadens the spectrum of FHL1-related disorders and implicates it in the pathogenesis of NS spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_provenance.
- NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_assertion evidence source_evidence_literature NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_provenance.
- NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_assertion SIO_000772 23456229 NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_provenance.
- NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_assertion wasDerivedFrom befree-20150227 NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_provenance.
- NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_assertion wasGeneratedBy ECO_0000203 NP403583.RA9wLXURt8at7l5JjPjQ8G81NhgSDLuYKH1bk4RJgFX5Y130_provenance.