Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.
- NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_assertion description "[The successful translation to clinical medicine of molecular genetic research on other rare monogenic metabolic disorders has stimulated the evaluation of such rare monogenic forms of insulin resistance as partial lipodystrophy resulting from mutations in either LMNA or PPARG genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.
- NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_assertion evidence source_evidence_literature NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.
- NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_assertion SIO_000772 15177263 NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.
- NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_assertion wasDerivedFrom befree-20140225 NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.
- NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_assertion wasGeneratedBy ECO_0000203 NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP484881.RAQNRWqtoSNhBVaB-JUCnqmV2eavFDgPItLhvNsIJCPRI130_provenance.