Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion wasGeneratedBy ECO_0000218 NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion wasDerivedFrom uniprot-2016 NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion SIO_000772 15562009 NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion evidence source_evidence_curated NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.
- NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_assertion description "[Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3761.RAe6nBSmT-uEQ8zkhIccZwiG2IuTRFZ0vmIYHpni3P4pc130_provenance.