Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.
- NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_assertion description "[Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.
- NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_assertion evidence source_evidence_literature NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.
- NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_assertion SIO_000772 14607793 NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.
- NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_assertion wasDerivedFrom gad-20150221 NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.
- NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_assertion wasGeneratedBy ECO_0000203 NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82462.RA7Z2qBLjhxk15toJ5PKMbPxyowluYK2-SUDnNPhTsGgg130_provenance.