Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.
- NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_assertion wasGeneratedBy ECO_0000218 NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.
- NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_assertion wasDerivedFrom uniprot-2016 NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.
- NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_assertion SIO_000772 15562009 NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.
- NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_assertion evidence source_evidence_curated NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.
- NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_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." NP3760.RAfieF6sfBkdW09nlph1LzBe98AF4fmWS4U-tWQjjv2HA130_provenance.