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- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion type Assertion NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_head.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion description "[Subsequent studies, however, found that UBQLN2 mutations were rare, and the pathogenicity of SIGMAR1 mutation in FTD and/or motor neuron disease was controversial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion evidence source_evidence_literature NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion SIO_000772 24684794 NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion wasDerivedFrom befree-20150227 NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion wasGeneratedBy ECO_0000203 NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.