Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
- NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_assertion wasGeneratedBy ECO_0000203 NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
- NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_assertion wasDerivedFrom befree-20140225 NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
- NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_assertion SIO_000772 8840534 NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
- NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_assertion evidence source_evidence_literature NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
- NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_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." NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP276087.RASWco25xeRwoo9kY6zTVOJOI1NyysaCNlGjoVXvruxWQ130_provenance.