Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.
- NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_assertion description "[These include the hyperinsulinism/hyperammonemia syndrome caused by dominant activating mutations of GLUD1 which interfere with inhibitory regulation by GTP and hyperinsulinism due to recessive deficiency of short-chain 3-hydroxy-acyl-CoA dehydrogenase (SCHAD, encoded by HADH1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.
- NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_assertion evidence source_evidence_literature NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.
- NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_assertion SIO_000772 21130127 NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.
- NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_assertion wasDerivedFrom befree-2016 NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.
- NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_assertion wasGeneratedBy ECO_0000203 NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.
- befree-2016 importedOn "2016-02-19" NP856892.RAcl8wsUU9M6l3b5maTLV873wJshnI6GBAxHiFhFkXGtw130_provenance.