Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_assertion> ?p ?o ?g. }
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- NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_assertion type Assertion NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_head.
- NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_assertion description "[Mutations in UBQLN2 encoding ubiquilin-2 have recently been identified in families with dominant X-linked juvenile and adult-onset amyotrophic lateral sclerosis (ALS) and ALS/dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_provenance.
- NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_assertion evidence source_evidence_literature NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_provenance.
- NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_assertion SIO_000772 22169395 NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_provenance.
- NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_assertion wasDerivedFrom befree-20150227 NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_provenance.
- NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_assertion wasGeneratedBy ECO_0000203 NP895440.RACfzFiokV9R14Ji5Vy_3JTvBB5EAgcBKz_GVr4c5OBYg130_provenance.