Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_assertion> ?p ?o ?g. }
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- NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_assertion type Assertion NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_head.
- NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_assertion description "[Variants identified through this study were previously reported to be involved in FTD and/or MND, but we are the first to describe their effects as potential disease modifiers in the presence of a clear pathogenic mutation (i.e.C9ORF72 repeat expansion).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_provenance.
- NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_assertion evidence source_evidence_literature NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_provenance.
- NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_assertion SIO_000772 25239657 NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_provenance.
- NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_assertion wasDerivedFrom befree-2016 NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_provenance.
- NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_assertion wasGeneratedBy ECO_0000203 NP1222099.RAmIQJsuHZp_I7PJzUnFWBh-D0Pbyu8rAERHfrED-OalE130_provenance.