Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- befree-20150227 importedOn "2015-02-27" NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion wasGeneratedBy ECO_0000203 NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion wasDerivedFrom befree-20150227 NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion SIO_000772 24684794 NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_assertion evidence source_evidence_literature NP840230.RAxhrN9tm-8zvBEVNZoE9znlTqKUzQA3IPVifxWpPti14130_provenance.
- 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.