Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_assertion> ?p ?o ?g. }
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- NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_assertion type Assertion NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_head.
- NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_assertion wasGeneratedBy ECO_0000203 NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_provenance.
- NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_assertion wasDerivedFrom befree-2016 NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_provenance.
- NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_assertion SIO_000772 24344182 NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_provenance.
- NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_assertion evidence source_evidence_literature NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_provenance.
- NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_assertion description "[Septin 9 (SEPT9) interacts with microtubules (MTs) and is mutated in hereditary neuralgic amyotrophy (HNA), an autosomal-dominant neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1137429.RAfGEzCK0lmeqhxk5R9VYRdmCJKk0nWNnJ3OXxYYk_NkA130_provenance.