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- NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_assertion type Assertion NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_head.
- NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_assertion wasGeneratedBy ECO_0000203 NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_provenance.
- NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_assertion wasDerivedFrom befree-20150227 NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_provenance.
- NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_assertion SIO_000772 14967765 NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_provenance.
- NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_assertion evidence source_evidence_literature NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_provenance.
- NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_assertion description "[At the same time, this progress blurs the traditional boundaries between the categories of congenital and limb-girdle muscular dystrophies, as well as between limb-girdle muscular dystrophies and other clinical entities, as mutations in genes such as fukutin-related protein, dysferlin, caveolin-3 and lamin A/C can cause a striking variety of phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284458.RA36Huemv8xmHb1qTm7-W4nWOHUvl76Q3GbtOBfOP3EPk130_provenance.