Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion> ?p ?o ?g. }
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- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion type Assertion NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_head.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion wasGeneratedBy ECO_0000218 NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion wasDerivedFrom ctd_human-20130708 NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion SIO_000772 22961002 NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion evidence source_evidence_curated NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.
- NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_assertion description "[Our study provides evidence that loss of functional HINT1 protein results in a distinct phenotype of autosomal recessive axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP17892.RAkr5-3N7qN-ZPb1soB50yp4Ulz0a-Ac4mDw6DRdQedb8130_provenance.