Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_assertion type Assertion NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_head.
- NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_assertion description "[Although ubiquitously expressed, DNM2 was found mutated in two genetic disorders affecting different tissues: autosomal dominant centronuclear myopathy (ADCNM; skeletal muscle) and peripheral Charcot-Marie-Tooth neuropathy (peripheral nerve).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_provenance.
- NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_assertion evidence source_evidence_literature NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_provenance.
- NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_assertion SIO_000772 21514436 NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_provenance.
- NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_assertion wasDerivedFrom befree-20150227 NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_provenance.
- NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_assertion wasGeneratedBy ECO_0000203 NP357074.RATdAf2qoLMMW7YJbbCbK9rzfUpogRwmOaIFAn1KJkYmU130_provenance.