Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.
- NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_assertion wasGeneratedBy ECO_0000203 NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.
- NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_assertion wasDerivedFrom befree-20150227 NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.
- NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_assertion SIO_000772 20370797 NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.
- NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_assertion evidence source_evidence_literature NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.
- NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_assertion description "[Genetic studies were performed to detect mutations in the SLC22A5 for primary carnitine deficiency, PNPLA2 for neutral lipid storage disease with myopathy, ABHD5 for neutral lipid storage disease with ichthyosis, ETFDH for multiple acyl-CoA dehydrogenation deficiency (MADD), and CPT2 for carnitine palmitoyltransferase II deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324628.RA1YE_dE4FevBwS6seV5v91HGOu5YMRbbnK2xrIwQ1qJg130_provenance.