Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_assertion> ?p ?o ?g. }
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- NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_assertion type Assertion NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_head.
- NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_assertion wasGeneratedBy ECO_0000203 NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_provenance.
- NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_assertion wasDerivedFrom befree-2016 NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_provenance.
- NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_assertion SIO_000772 14967765 NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_provenance.
- NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_assertion evidence source_evidence_literature NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_provenance.
- NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_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." NP431989.RAEeGX5eCift1PBfuYsD6CO_FJiXV2zXtBLqv3nfr6hmA130_provenance.