Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_assertion type Assertion NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_head.
- NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_assertion description "[Defects in the nuclear envelope protein lamin A/C, encoded by the LMNA gene, have been shown to be associated with a variety of disorders affecting mainly the muscular and adipose tissues and, more recently, with autosomal recessive Charcot-Marie-Tooth type 2 neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_provenance.
- NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_assertion evidence source_evidence_literature NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_provenance.
- NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_assertion SIO_000772 15965218 NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_provenance.
- NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_assertion wasDerivedFrom befree-2016 NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_provenance.
- NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_assertion wasGeneratedBy ECO_0000203 NP500163.RAXgI1V6YZ8iz7JeDQ9apv-GsyMDdAeHMjcE6-L1cPBLc130_provenance.