Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion> ?p ?o ?g. }
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- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion type Assertion NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_head.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion wasGeneratedBy ECO_0000218 NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion wasDerivedFrom uniprot-20150221 NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion SIO_000772 22961002 NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion evidence source_evidence_curated NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_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." NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.