Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_assertion> ?p ?o ?g. }
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- NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_assertion type Assertion NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_head.
- NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_assertion description "[An expanded hexanucleotide repeat in the C9orf72 gene is the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia (C9ALS/FTD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_provenance.
- NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_assertion evidence source_evidence_literature NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_provenance.
- NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_assertion SIO_000772 25179228 NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_provenance.
- NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_assertion wasDerivedFrom befree-2016 NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_provenance.
- NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_assertion wasGeneratedBy ECO_0000203 NP1216019.RAZCnkS7q1qhfnEu3Kbu0LxnIJB6EpiUtOjbNjEdhdxec130_provenance.