Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_assertion type Assertion NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_head.
- NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_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." NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_provenance.
- NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_assertion evidence source_evidence_literature NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_provenance.
- NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_assertion SIO_000772 25342199 NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_provenance.
- NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_assertion wasDerivedFrom befree-2016 NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_provenance.
- NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_assertion wasGeneratedBy ECO_0000203 NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_provenance.