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- source_evidence_literature type ECO_0000212 NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.
- NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_assertion wasGeneratedBy ECO_0000203 NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.
- NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_assertion wasDerivedFrom befree-2016 NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.
- NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_assertion SIO_000772 8840534 NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.
- NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_assertion evidence source_evidence_literature NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.
- NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_assertion description "[The prevalence of the 985A-to-G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidation disorders and severe motor and intellectual disabilities was studied using the PCR/Nco-I method for molecular diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1359071.RArXbWNi4YFDWEAXoreduzcrMRpkfhMCfGK3sQ-cCol-k130_provenance.