Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.
- NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_assertion description "[Similarly, incubating LCHAD and MTP deficient cell lines with the long-chain branched fatty acid, pristanic acid, and monitoring the C11/C9 acylcarnitine ratio has allowed differentiation between these disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.
- NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_assertion evidence source_evidence_literature NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.
- NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_assertion SIO_000772 16297647 NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.
- NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_assertion wasDerivedFrom befree-2016 NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.
- NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_assertion wasGeneratedBy ECO_0000203 NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.
- befree-2016 importedOn "2016-02-19" NP523225.RAckgV0O1FJK-dd9QFWcnjkcx71HIydohg0GoeL8bVFwE130_provenance.