Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.
- NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_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." NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.
- NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_assertion evidence source_evidence_literature NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.
- NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_assertion SIO_000772 23273570 NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.
- NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_assertion wasDerivedFrom befree-2016 NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.
- NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_assertion wasGeneratedBy ECO_0000203 NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1039188.RAl8rgN3T8PzQ63UYoS4htY9IfJDLZNFUi5wfb4HzgFj4130_provenance.