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- source_evidence_literature type ECO_0000212 NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP870800.RA1hTGyfpCEMM4NcLn4rFdedO9_NNZ66c9u41omZDukbg130_provenance.