Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_assertion> ?p ?o ?g. }
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- NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_assertion type Assertion NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_head.
- NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_assertion description "[The discovery of the c.1054C>T; p.R352W mutation in the FOXRED1 gene is a further contribution towards resolving the complex puzzle of the genetic basis of human mitochondrial disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.
- NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_assertion evidence source_evidence_literature NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.
- NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_assertion SIO_000772 20858599 NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.
- NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_assertion wasDerivedFrom befree-20140225 NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.
- NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_assertion wasGeneratedBy ECO_0000203 NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.