Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion> ?p ?o ?g. }
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- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion type Assertion NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_head.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion description "[Mutations of the lamin A/C gene are associated with several different neuromuscular diseases, and the detailed effect of disease-associated amino acid substitutions on the structure and stability of human lamin dimers is yet unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion evidence source_evidence_literature NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion SIO_000772 23142632 NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion wasDerivedFrom befree-20150227 NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.
- NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_assertion wasGeneratedBy ECO_0000203 NP537512.RAeJpSOGtEdJL6z6IuGvw7PWaidFSE4kQsoIRjHwrRSYI130_provenance.