Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.
- NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_assertion description "[We report an infant presenting with afebrile seizures secondary to hyperinsulinemic hypoglycemia resulting from a novel de novo mutation of the GLUD1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.
- NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_assertion evidence source_evidence_literature NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.
- NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_assertion SIO_000772 21932603 NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.
- NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_assertion wasDerivedFrom befree-2016 NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.
- NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_assertion wasGeneratedBy ECO_0000203 NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.
- befree-2016 importedOn "2016-02-19" NP925048.RAJSbdeZa3fNbtZRKX9Qmwq6tC_KRAVpqjw_cPpX5JImE130_provenance.