Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_assertion> ?p ?o ?g. }
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- NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_assertion type Assertion NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_head.
- NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_provenance.
- NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_assertion evidence source_evidence_literature NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_provenance.
- NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_assertion SIO_000772 25342199 NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_provenance.
- NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_assertion wasDerivedFrom befree-2016 NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_provenance.
- NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_assertion wasGeneratedBy ECO_0000203 NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_provenance.