Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_assertion> ?p ?o ?g. }
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- NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_assertion type Assertion NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_head.
- NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_assertion description "[Hereditary sensory neuropathy type I (HSN I) is an axonal form of autosomal-dominant hereditary motor and sensory neuropathy distinguished by prominent sensory loss that leads to painless injuries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_provenance.
- NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_assertion evidence source_evidence_literature NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_provenance.
- NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_assertion SIO_000772 21194679 NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_provenance.
- NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_assertion wasDerivedFrom befree-2016 NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_provenance.
- NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_assertion wasGeneratedBy ECO_0000203 NP862310.RAVt5EK5uYPaJcSVkO3BVAq0Pfwxq3CubrUWyqm7KEAjU130_provenance.