Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.
- NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_assertion description "[We investigated individuals with hyperinsulinaemic hypoglycaemia and biochemical or genetic evidence to suggest noncoding mutations by using NGS to analyze the entire genomic regions of ABCC8 (117 kb) and HADH (94 kb) from overlapping ~10 kb PCR amplicons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.
- NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_assertion evidence source_evidence_literature NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.
- NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_assertion SIO_000772 23273570 NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.
- NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_assertion wasDerivedFrom befree-20150227 NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.
- NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_assertion wasGeneratedBy ECO_0000203 NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443231.RAWXfPy_maXC2HUiV75l4UtWRwpZRrvBhlOYwkRCN_PLY130_provenance.