Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_assertion> ?p ?o ?g. }
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- NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_assertion type Assertion NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_head.
- NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_assertion wasGeneratedBy ECO_0000203 NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_provenance.
- NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_assertion wasDerivedFrom befree-20150227 NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_provenance.
- NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_assertion SIO_000772 22961002 NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_provenance.
- NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_assertion evidence source_evidence_literature NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_provenance.
- NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450379.RAo38R5ACdyZZ7X7xBO7_j_gZcR8JLRgK4FQuuK2aA9NU130_provenance.