Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.
- NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_assertion wasGeneratedBy ECO_0000203 NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.
- NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_assertion wasDerivedFrom befree-20150227 NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.
- NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_assertion SIO_000772 25008398 NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.
- NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_assertion evidence source_evidence_literature NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.
- NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_assertion description "[To establish the phenotypic spectrum of KIF5A mutations and to investigate whether KIF5A mutations cause axonal neuropathy associated with hereditary spastic paraplegia (HSP) or typical Charcot-Marie-Tooth disease type 2 (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524188.RACIyouvAL7olcVg1XbRNrrL8VLVGmMZmJE_zXKAkXiM8130_provenance.