Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_assertion> ?p ?o ?g. }
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- NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_assertion type Assertion NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_head.
- NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_assertion description "[Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_provenance.
- NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_assertion evidence source_evidence_literature NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_provenance.
- NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_assertion SIO_000772 14607793 NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_provenance.
- NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_assertion wasDerivedFrom befree-20150227 NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_provenance.
- NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_assertion wasGeneratedBy ECO_0000203 NP537321.RAGyDHXhiaphhZc07xoA82DIbvf2bj-xgGMnp1ny_VK5Q130_provenance.