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- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion type Assertion NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_head.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_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." NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion evidence source_evidence_literature NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion SIO_000772 23456229 NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion wasDerivedFrom befree-20150227 NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.
- NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_assertion wasGeneratedBy ECO_0000203 NP887710.RA818yNU8rLN04z4AnkazxwNI9QSI8gEUGvkvvjII9CME130_provenance.