Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.
- NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_assertion description "[Usher type 1C maps to the region containing the genes ABCC8 and KCNJ11 (encoding components of ATP-sensitive K + (KATP) channels), which may be mutated in patients with hyperinsulinism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.
- NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_assertion evidence source_evidence_literature NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.
- NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_assertion SIO_000772 10973248 NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.
- NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_assertion wasDerivedFrom befree-20150227 NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.
- NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_assertion wasGeneratedBy ECO_0000203 NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP522683.RAPY0L4zOCO14W8MByjfgMSKGBmmP0XYPk2YeEMMSCtzI130_provenance.