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- NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_assertion type Assertion NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_head.
- NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_assertion description "[Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_provenance.
- NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_assertion evidence source_evidence_literature NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_provenance.
- NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_assertion SIO_000772 25342199 NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_provenance.
- NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_assertion wasDerivedFrom befree-2016 NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_provenance.
- NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_assertion wasGeneratedBy ECO_0000203 NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_provenance.