Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_assertion> ?p ?o ?g. }
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- NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_assertion type Assertion NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_head.
- NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_assertion description "[Our findings show the difficulty in distinguishing CMTX patients from CMT1 and CMT2 patients, and they emphasize the need for Cx32 mutation screening in families previously diagnosed with CMT2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_provenance.
- NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_assertion evidence source_evidence_curated NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_provenance.
- NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_assertion SIO_000772 9272161 NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_provenance.
- NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_assertion wasDerivedFrom uniprot-2016 NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_provenance.
- NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_assertion wasGeneratedBy ECO_0000218 NP9471.RATuuwQZy-LKnfsbOObuPpiDFF8A2NbfLlaoN98SMrHzM130_provenance.